ACTIVE ADAPTER

Electrosurgical, Cutting & Coagulation & Accessories

BEACON LABORATORIES, INC.

The following data is part of a premarket notification filed by Beacon Laboratories, Inc. with the FDA for Active Adapter.

Pre-market Notification Details

Device IDK904506
510k NumberK904506
Device Name:ACTIVE ADAPTER
ClassificationElectrosurgical, Cutting & Coagulation & Accessories
Applicant BEACON LABORATORIES, INC. 2150 WEST 6TH AVE., UNIT P Broomfield,  CO  80020
ContactJohn Etter
CorrespondentJohn Etter
BEACON LABORATORIES, INC. 2150 WEST 6TH AVE., UNIT P Broomfield,  CO  80020
Product CodeGEI  
CFR Regulation Number878.4400 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1990-10-02
Decision Date1990-12-13

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.