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FDA 510(k)

STERILIZATION PROCESS/PLACENTA BASIN

K-Number: K792625 · 1980-01-16

ApplicantProcter & Gamble Mfg. Co.
Decision Date1980-01-16
Product CodeFNY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STERILIZATION PROCESS/PLACENTA BASIN is the device name listed in this FDA 510(k) record. The listed applicant is Procter & Gamble Mfg. Co.. It received FDA 510(k) clearance on 1980-01-16 under 510(k) number K792625. The device is classified under product code FNY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERILIZATION PROCESS/PLACENTA BASIN?

STERILIZATION PROCESS/PLACENTA BASIN is a medical device that received FDA 510(k) clearance on 1980-01-16. The listed applicant is Procter & Gamble Mfg. Co.. The 510(k) number is K792625.

When did STERILIZATION PROCESS/PLACENTA BASIN receive FDA 510(k) clearance?

STERILIZATION PROCESS/PLACENTA BASIN received FDA 510(k) clearance on 1980-01-16, under 510(k) number K792625.

Who is the listed applicant for STERILIZATION PROCESS/PLACENTA BASIN?

The FDA 510(k) record lists Procter & Gamble Mfg. Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STERILIZATION PROCESS/PLACENTA BASIN?

The FDA product code for STERILIZATION PROCESS/PLACENTA BASIN is FNY.

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Other records listing Procter & Gamble Mfg. Co. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: FNY)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K832826AAP DOSIMETRY RELEASE OR BASIN SETSAmerican Hospital Supply Corp.K802538BASIN PACKTexas Medical Products, Inc.K800440STERILE SPONGE BOWLSPremium Plastics, Inc.K7717338 EMESIS BASINBemis Health CareK760494BASIN, ROUND WASHLandmark PlasticsK760495BASIN, RECTANGULAR WASHLandmark Plastics

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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