WHITE KNIGHT BOVIE CORD/SUCTION TUBE

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 Bovie Cord/suction Tube.

Pre-market Notification Details

Device IDK802213
510k NumberK802213
Device Name:WHITE KNIGHT BOVIE CORD/SUCTION TUBE
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 Received1980-09-12
Decision Date1980-10-10

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