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FDA 510(k)

BOUNDARY EXTREMITY DRAPE

K-Number: K801132 · 1980-05-20

ApplicantProcter & Gamble Mfg. Co.
Decision Date1980-05-20
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BOUNDARY EXTREMITY DRAPE 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 1980-05-20 under 510(k) number K801132. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BOUNDARY EXTREMITY DRAPE?

BOUNDARY EXTREMITY DRAPE is a medical device that received FDA 510(k) clearance on 1980-05-20. The listed applicant is Procter & Gamble Mfg. Co.. The 510(k) number is K801132.

When did BOUNDARY EXTREMITY DRAPE receive FDA 510(k) clearance?

BOUNDARY EXTREMITY DRAPE received FDA 510(k) clearance on 1980-05-20, under 510(k) number K801132.

Who is the listed applicant for BOUNDARY EXTREMITY DRAPE?

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 BOUNDARY EXTREMITY DRAPE?

The FDA product code for BOUNDARY EXTREMITY DRAPE is KKX.

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

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Related Devices (Code: KKX)

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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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