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FDA 510(k)

STERILIZATION PROCESS/BULB SYRINGE

K-Number: K792632 · 1980-01-16

ApplicantProcter & Gamble Mfg. Co.
Decision Date1980-01-16
Product Code
DecisionSubstantially Equivalent

Device Summary

STERILIZATION PROCESS/BULB SYRINGE 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 K792632. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERILIZATION PROCESS/BULB SYRINGE?

STERILIZATION PROCESS/BULB SYRINGE 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 K792632.

When did STERILIZATION PROCESS/BULB SYRINGE receive FDA 510(k) clearance?

STERILIZATION PROCESS/BULB SYRINGE received FDA 510(k) clearance on 1980-01-16, under 510(k) number K792632.

Who is the listed applicant for STERILIZATION PROCESS/BULB SYRINGE?

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

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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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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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