ZEE SURGICAL INSTRUMENTS

Handle, Scalpel

ZEE MEDICAL PRODUCTS CO., INC.

The following data is part of a premarket notification filed by Zee Medical Products Co., Inc. with the FDA for Zee Surgical Instruments.

Pre-market Notification Details

Device IDK812814
510k NumberK812814
Device Name:ZEE SURGICAL INSTRUMENTS
ClassificationHandle, Scalpel
Applicant ZEE MEDICAL PRODUCTS CO., INC. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeGDZ  
CFR Regulation Number878.4800 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1981-10-06
Decision Date1981-11-06

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