STERILIZATION PROCESS/VAGINAL SPONGE
K-Number: K792628 · 1980-01-11
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Device Summary
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.
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
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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