PREVU POINT OF CARE SKIN STEROL TEST— 510(k) K062092

Unknown

Premd, Inc.

FDA 510(k) clearance K062092 for PREVU POINT OF CARE SKIN STEROL TEST, Unknown on 2006-09-15. Applicant: Premd, Inc.. Device class: 1.

Clearance details

Applicant: Premd, Inc.
Product code: Code LBS
Device class: Class 1
Regulation: 21 CFR 862.1475
Advisory panel: Clinical Chemistry
Date received: 2006-07-24
Decision date: 2006-09-15
Decision: Unknown
Clearance type: Special
Location: Rockville, MD, US

Download summary PDF View on FDA.gov ↗

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