K792632Substantially Equivalent

Sterilization Process/bulb Syringe

Name: K792632 Sterilization Process/bulb Syringe
Creator: Procter & Gamble Mfg. Co.
Published: 1980-01-16
License: https://open.fda.gov/license/

Procter & Gamble Mfg. Co., Mchenry IL / Traditional, Substantially Equivalent

FDA source

K792632 is the FDA 510(k) clearance record for STERILIZATION PROCESS/BULB SYRINGE, cleared for Procter & Gamble Mfg. Co. on 1980-01-16. FDA records list 72 510(k) clearances for Procter & Gamble Mfg. Co., from 1976-08-11 to 1988-01-19. As of 2026-09-10, FDA records show no recalls naming K792632.

Clearance record

Decision date: 1980-01-16
Received: 1979-12-19 (28 days to decision)
Review panel: Unknown
Applicant: Procter & Gamble Mfg. Co. 803 N. Front St. Suite 3, Mchenry IL
Third party review: No