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FDA 510(k)

STERILIZATION PROCESS/DBL. GRIP CORD CLP

K-Number: K792631 · 1980-01-28

ApplicantProcter & Gamble Mfg. Co.
Decision Date1980-01-28
Product CodeKNA
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

STERILIZATION PROCESS/DBL. GRIP CORD CLP 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 1980-01-28 under 510(k) number K792631. The device is classified under product code KNA. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERILIZATION PROCESS/DBL. GRIP CORD CLP?

STERILIZATION PROCESS/DBL. GRIP CORD CLP is a medical device that received FDA 510(k) clearance on 1980-01-28. The listed applicant is Procter & Gamble Mfg. Co.. The 510(k) number is K792631.

When did STERILIZATION PROCESS/DBL. GRIP CORD CLP receive FDA 510(k) clearance?

STERILIZATION PROCESS/DBL. GRIP CORD CLP received FDA 510(k) clearance on 1980-01-28, under 510(k) number K792631.

Who is the listed applicant for STERILIZATION PROCESS/DBL. GRIP CORD CLP?

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/DBL. GRIP CORD CLP?

The FDA product code for STERILIZATION PROCESS/DBL. GRIP CORD CLP is KNA.

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

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Related Devices (Code: KNA)

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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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