HM-880 I

Electrosurgical, Cutting & Coagulation & Accessories

HILL-MED, INC.

The following data is part of a premarket notification filed by Hill-med, Inc. with the FDA for Hm-880 I.

Pre-market Notification Details

Device IDK932817
510k NumberK932817
Device Name:HM-880 I
ClassificationElectrosurgical, Cutting & Coagulation & Accessories
Applicant HILL-MED, INC. 7217 N.W. 46TH ST. Miami,  FL  33166
ContactErnesto Ackerman
CorrespondentErnesto Ackerman
HILL-MED, INC. 7217 N.W. 46TH ST. Miami,  FL  33166
Product CodeGEI  
CFR Regulation Number878.4400 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1993-06-09
Decision Date1994-03-09

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