FDA 510(k)

WHITE KNIGHT DRAPE SEAL

K-Number: K802280 · 1980-10-10

Decision Date1980-10-10

Product CodeKKX

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

WHITE KNIGHT DRAPE SEAL 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 1980-10-10 under 510(k) number K802280. 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 DRAPE SEAL?

WHITE KNIGHT DRAPE SEAL is a medical device that received FDA 510(k) clearance on 1980-10-10. The listed applicant is G.D. Searle and Co.. The 510(k) number is K802280.

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

WHITE KNIGHT DRAPE SEAL received FDA 510(k) clearance on 1980-10-10, under 510(k) number K802280.

Who is the listed applicant for WHITE KNIGHT DRAPE SEAL?

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 DRAPE SEAL?

The FDA product code for WHITE KNIGHT DRAPE SEAL 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.