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FDA 510(k)

STERILIZATION PROCESS/VAGINAL SPONGE

K-Number: K792628 · 1980-01-11

Decision Date1980-01-11
Product CodeEFQ
DecisionSubstantially Equivalent

Device Summary

STERILIZATION PROCESS/VAGINAL SPONGE 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 1980-01-11 under 510(k) number K792628. The device is classified under product code EFQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERILIZATION PROCESS/VAGINAL SPONGE?

STERILIZATION PROCESS/VAGINAL SPONGE is a medical device that received FDA 510(k) clearance on 1980-01-11. The listed applicant is Procter & Gamble Mfg. Co.. The 510(k) number is K792628.

When did STERILIZATION PROCESS/VAGINAL SPONGE receive FDA 510(k) clearance?

STERILIZATION PROCESS/VAGINAL SPONGE received FDA 510(k) clearance on 1980-01-11, under 510(k) number K792628.

Who is the listed applicant for STERILIZATION PROCESS/VAGINAL SPONGE?

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/VAGINAL SPONGE?

The FDA product code for STERILIZATION PROCESS/VAGINAL SPONGE is EFQ.

Related Clinical Trials

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.

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.

View all 72 devices →

Related Devices (Code: EFQ)

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.

Official Source

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

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