BOUNDARY EXTREMITY DRAPE— 510(k) K801132

Name: FDA 510(k) clearance K801132
Creator: U.S. Food and Drug Administration
Published: 1980-05-20

Substantially Equivalent

Procter & Gamble Mfg. Co.

FDA 510(k) clearance K801132 for BOUNDARY EXTREMITY DRAPE, Substantially Equivalent on 1980-05-20. Applicant: Procter & Gamble Mfg. Co.. Device class: 2.

Clearance details

Applicant: Procter & Gamble Mfg. Co.
Product code: Code KKX
Device class: Class 2
Regulation: 21 CFR 878.4370
Advisory panel: General, Plastic Surgery
Date received: 1980-05-12
Decision date: 1980-05-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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