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

PRESSURE GUARD

K Number: K913772 · Decision Nov 19, 1991
Classifications
1
FEI Numbers
141
Registration Numbers
141
Same Product Code
176
Applicant Total
18
Review Days
88

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Basic Information

Device Name
PRESSURE GUARD
K Number
K913772
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1730
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Beacon Laboratories, Inc.
Date Received
August 23, 1991
Decision Date
November 19, 1991
Product Code
HIF
Advisory Committee
Obstetrics/Gynecology
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
HIF Insufflator, Laparoscopic

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K925619 DISPOSABLE HAND-SWITCHING ESU PENCIL
K915788 MIS ELECTROSURGICAL ELECTRODES
K920100 GSU HANDPIECE ADAPTER
K905752 ARGON BEAM COMBO LAPAROSCOPIC ELECTRODE
K904506 ACTIVE ADAPTER
K902996 ARGON BEAM LAPAROSCOPIC ELECTRODE
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