WHITE KNIGHT SUPPLEMENTAL DRAPE

Drape, Surgical

G.D. SEARLE AND CO.

The following data is part of a premarket notification filed by G.d. Searle And Co. with the FDA for White Knight Supplemental Drape.

Pre-market Notification Details

Device IDK800928
510k NumberK800928
Device Name:WHITE KNIGHT SUPPLEMENTAL DRAPE
ClassificationDrape, Surgical
Applicant G.D. SEARLE AND CO. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeKKX  
CFR Regulation Number878.4370 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1980-04-21
Decision Date1980-05-20

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