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

Precise SHP Diode Laser

K Number: K181601 · Decision Sep 9, 2019
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
9
Review Days
447

Basic Information

Device Name
Precise SHP Diode Laser
K Number
K181601
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4810
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
CAO Group, Inc.
Date Received
June 19, 2018
Decision Date
September 9, 2019
Product Code
GEX
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
GEX Powered Laser Surgical Instrument

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