FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

B1 FOOTSWITCH (SINGLE PEDDLE), B2 (DOUBLE PEDDLE)

K Number: K894602 · Decision Aug 9, 1989
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
18
Review Days
20

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Basic Information

Device Name
B1 FOOTSWITCH (SINGLE PEDDLE), B2 (DOUBLE PEDDLE)
K Number
K894602
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Beacon Laboratories, Inc.
Date Received
July 20, 1989
Decision Date
August 9, 1989
Product Code
GEI
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

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K922289 SESQUIPOLAR(TM) MIS ELECTRODE
K925619 DISPOSABLE HAND-SWITCHING ESU PENCIL
K915788 MIS ELECTROSURGICAL ELECTRODES
K920100 GSU HANDPIECE ADAPTER
K913772 PRESSURE GUARD
K905752 ARGON BEAM COMBO LAPAROSCOPIC ELECTRODE
K904506 ACTIVE ADAPTER
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