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FDA PRODUCT CODE · CLASS II

PTH — Test, Barbiturate, Over The Counter

The barbiturate test is an in vitro diagnostic test for the qualitative analysis of barbiturates in human urine.

DEVICE CLASS
Class II
REGULATION
21 CFR 862.3150
MEDICAL SPECIALTY
Clinical Toxicology
REVIEW PANEL
TX
— Implant— Life-sustaining— GMP-exempt✓ Third-party review eligible
0
510(K)/PMA CLEARANCES
0
RECALL ENTRIES

Related on SPEQ

Medical devices industry →Medical device quality (ISO 13485) →FDA device clearances →FDA enforcement & recalls →

Source: FDA device classification, 510(k)/PMA, and recall datasets (openFDA). Recall entries count distinct FDA recall numbers, so one recall event affecting several products appears as several entries. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data.

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