STERILIZATION PROCESS/DBL. GRIP CORD CLP— 510(k) K792631

Name: FDA 510(k) clearance K792631
Creator: U.S. Food and Drug Administration
Published: 1980-01-28

Substantially Equivalent

Procter & Gamble Mfg. Co.

FDA 510(k) clearance K792631 for STERILIZATION PROCESS/DBL. GRIP CORD CLP, Substantially Equivalent on 1980-01-28. Applicant: Procter & Gamble Mfg. Co.. Device class: 2.

Clearance details

Applicant: Procter & Gamble Mfg. Co.
Product code: Code KNA
Device class: Class 2
Regulation: 21 CFR 884.4530
Advisory panel: Obstetrics/Gynecology
Date received: 1979-12-19
Decision date: 1980-01-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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