HCPCS Level II
Temporary national codes
Letter S, 533 codes. CMS HCPCS Level II file dated September 23, 2026.
License: a US government work, in the public domain (Public Domain Mark 1.0).
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Codes matching S3
1 to 34 of 34
- S3000Diabetic indicator; retinal eye exam, dilated, bilateral
- S3005Performance measurement, evaluation of patient self assessment, depression
- S3600Stat laboratory request (situations other than s3601)
- S3601Emergency stat laboratory charge for patient who is homebound or residing in a nursing facility
- S3620Newborn metabolic screening panel, includes test kit, postage and the laboratory tests specified by the state for inclusion in this panel (e.g., galactose; hemoglobin, electrophoresis; hydroxyprogesterone, 17-d; phenylalanine (pku); and thyroxine, total)
- S3630Eosinophil count, blood, direct
- S3645Hiv-1 antibody testing of oral mucosal transudate
- S3650Saliva test, hormone level; during menopause
- S3652Saliva test, hormone level; to assess preterm labor risk
- S3655Antisperm antibodies test (immunobead)
- S3708Gastrointestinal fat absorption study
- S3721Prostate cancer antigen 3 (pca3) testingDeleted 2015
- S3722Dose optimization by area under the curve (auc) analysis, for infusional 5-fluorouracil
- S3800Genetic testing for amyotrophic lateral sclerosis (als)
- S3840Dna analysis for germline mutations of the ret proto-oncogene for susceptibility to multiple endocrine neoplasia type 2
- S3841Genetic testing for retinoblastoma
- S3842Genetic testing for von hippel-lindau disease
- S3844Dna analysis of the connexin 26 gene (gjb2) for susceptibility to congenital, profound deafness
- S3845Genetic testing for alpha-thalassemia
- S3846Genetic testing for hemoglobin e beta-thalassemia
- S3849Genetic testing for niemann-pick disease
- S3850Genetic testing for sickle cell anemia
- S3852Dna analysis for apoe epsilon 4 allele for susceptibility to alzheimer's disease
- S3853Genetic testing for myotonic muscular dystrophy
- S3854Gene expression profiling panel for use in the management of breast cancer treatment
- S3855Genetic testing for detection of mutations in the presenilin - 1 geneDeleted 2014
- S3861Genetic testing, sodium channel, voltage-gated, type v, alpha subunit (scn5a) and variants for suspected brugada syndrome
- S3865Comprehensive gene sequence analysis for hypertrophic cardiomyopathy
- S3866Genetic analysis for a specific gene mutation for hypertrophic cardiomyopathy (hcm) in an individual with a known hcm mutation in the family
- S3870Comparative genomic hybridization (cgh) microarray testing for developmental delay, autism spectrum disorder and/or intellectual disability
- S3890Dna analysis, fecal, for colorectal cancer screeningDeleted 2015
- S3900Surface electromyography (emg)
- S3902Ballistocardiogram
- S3904Masters two step