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

ABC HANDPIECE ADAPTER

K Number: K901248 · Decision Apr 3, 1990
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
30
Applicant Total
18
Review Days
19

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Basic Information

Device Name
ABC HANDPIECE ADAPTER
K Number
K901248
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
March 15, 1990
Decision Date
April 3, 1990
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
K920100 GSU HANDPIECE ADAPTER
K913772 PRESSURE GUARD
K905752 ARGON BEAM COMBO LAPAROSCOPIC ELECTRODE
K904506 ACTIVE ADAPTER
Search all 18 clearances from Beacon Laboratories, Inc. →