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

ARGON HANDPIECES

K Number: K930497 · Decision Jun 25, 1993
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
18
Review Days
144

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Basic Information

Device Name
ARGON HANDPIECES
K Number
K930497
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
February 1, 1993
Decision Date
June 25, 1993
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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Other Clearances by Beacon Laboratories, Inc.

K Number Device Name
K930243 FLEXIBLE EXTENDER
K925708 DISPOSABLE ELECTROSURGERY BALL ELECTRODE
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
K902996 ARGON BEAM LAPAROSCOPIC ELECTRODE
Search all 18 clearances from Beacon Laboratories, Inc. →