STERILIZATION PROCESS/OUTERWRAP— 510(k) K792633

Name: FDA 510(k) clearance K792633
Creator: U.S. Food and Drug Administration
Published: 1980-01-11

Substantially Equivalent

Procter & Gamble Mfg. Co.

FDA 510(k) clearance K792633 for STERILIZATION PROCESS/OUTERWRAP, Substantially Equivalent on 1980-01-11. Applicant: Procter & Gamble Mfg. Co.. Device class: 1.

Clearance details

Applicant: Procter & Gamble Mfg. Co.
Product code: Code KET
Device class: Class 1
Regulation: 21 CFR 864.3010
Advisory panel: Pathology
Date received: 1979-12-19
Decision date: 1980-01-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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