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

GSU HANDPIECE ADAPTER

K Number: K920100 · Decision Feb 3, 1992
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
30
Applicant Total
18
Review Days
25

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Basic Information

Device Name
GSU HANDPIECE ADAPTER
K Number
K920100
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Beacon Laboratories, Inc.
Date Received
January 9, 1992
Decision Date
February 3, 1992
Product Code
HAM
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
HAM Apparatus, Electrosurgical

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Other Clearances by Beacon Laboratories, Inc.

K Number Device Name
K930243 FLEXIBLE EXTENDER
K930497 ARGON HANDPIECES
K925708 DISPOSABLE ELECTROSURGERY BALL ELECTRODE
K922289 SESQUIPOLAR(TM) MIS ELECTRODE
K925619 DISPOSABLE HAND-SWITCHING ESU PENCIL
K915788 MIS ELECTROSURGICAL ELECTRODES
K913772 PRESSURE GUARD
K905752 ARGON BEAM COMBO LAPAROSCOPIC ELECTRODE
K904506 ACTIVE ADAPTER
K902996 ARGON BEAM LAPAROSCOPIC ELECTRODE
Search all 18 clearances from Beacon Laboratories, Inc. →