FDA 510(k)

WHITE KNIGHT SUPPLEMENTAL DRAPE

K-Number: K800928 · 1980-05-20

Decision Date1980-05-20

Product CodeKKX

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

WHITE KNIGHT SUPPLEMENTAL DRAPE is the device name listed in this FDA 510(k) record. The listed applicant is G.D. Searle and Co.. It received FDA 510(k) clearance on 1980-05-20 under 510(k) number K800928. 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 WHITE KNIGHT SUPPLEMENTAL DRAPE?

WHITE KNIGHT SUPPLEMENTAL DRAPE is a medical device that received FDA 510(k) clearance on 1980-05-20. The listed applicant is G.D. Searle and Co.. The 510(k) number is K800928.

When did WHITE KNIGHT SUPPLEMENTAL DRAPE receive FDA 510(k) clearance?

WHITE KNIGHT SUPPLEMENTAL DRAPE received FDA 510(k) clearance on 1980-05-20, under 510(k) number K800928.

Who is the listed applicant for WHITE KNIGHT SUPPLEMENTAL DRAPE?

The FDA 510(k) record lists G.D. Searle and Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WHITE KNIGHT SUPPLEMENTAL DRAPE?

The FDA product code for WHITE KNIGHT SUPPLEMENTAL DRAPE is 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.