STERILIZATION PROCESS/VAGINAL SPONGE— 510(k) K792628

Name: FDA 510(k) clearance K792628
Creator: U.S. Food and Drug Administration
Published: 1980-01-11

Substantially Equivalent

Procter & Gamble Mfg. Co.

FDA 510(k) clearance K792628 for STERILIZATION PROCESS/VAGINAL SPONGE, Substantially Equivalent on 1980-01-11. Applicant: Procter & Gamble Mfg. Co.. Device class: Unclassified.

Clearance details

Applicant: Procter & Gamble Mfg. Co.
Product code: Code EFQ
Device class: Unclassified
Advisory panel: Unknown
Date received: 1979-12-19
Decision date: 1980-01-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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