HI-TEMP LOOPTIP SURGICAL CAUTERY

Electrosurgical, Cutting & Coagulation & Accessories

MEDICAL PRODUCTS DEVELOPMENT, INC.

The following data is part of a premarket notification filed by Medical Products Development, Inc. with the FDA for Hi-temp Looptip Surgical Cautery.

Pre-market Notification Details

Device IDK802330
510k NumberK802330
Device Name:HI-TEMP LOOPTIP SURGICAL CAUTERY
ClassificationElectrosurgical, Cutting & Coagulation & Accessories
Applicant MEDICAL PRODUCTS DEVELOPMENT, INC. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeGEI  
CFR Regulation Number878.4400 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1980-09-23
Decision Date1980-11-12

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