TBD

Electrosurgical, Cutting & Coagulation & Accessories

MEGADYNE MEDICAL PRODUCTS, INC.

The following data is part of a premarket notification filed by Megadyne Medical Products, Inc. with the FDA for Tbd.

Pre-market Notification Details

Device IDK972273
510k NumberK972273
Device Name:TBD
ClassificationElectrosurgical, Cutting & Coagulation & Accessories
Applicant MEGADYNE MEDICAL PRODUCTS, INC. 11506 SOUTH STATE ST. Draper,  UT  84020
ContactJohn W Smith
CorrespondentJohn W Smith
MEGADYNE MEDICAL PRODUCTS, INC. 11506 SOUTH STATE ST. Draper,  UT  84020
Product CodeGEI  
CFR Regulation Number878.4400 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1997-06-18
Decision Date1997-07-08
Summary:summary

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