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FDA PRODUCT CODE · CLASS I

PTC — Uric Acid Test System For At Home Prescription Use

For the quantitative measurement of uric acid in home use settings by patients diagnosed with gout. This device is for prescription use only.

DEVICE CLASS
Class I
REGULATION
21 CFR 862.1775
MEDICAL SPECIALTY
Clinical Chemistry
REVIEW PANEL
CH
— Implant— Life-sustaining— GMP-exempt✓ Third-party review eligible
1
510(K)/PMA CLEARANCES
510k: 1
0
RECALL ENTRIES

Recent clearances

K242209Apex BioTechnology Corp. · 510k2025-04-04

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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