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

MX-7000 MICROXEL

K Number: K111831 · Decision Dec 19, 2011
Classifications
1
FEI Numbers
57
Registration Numbers
57
Same Product Code
34
Applicant Total
10
Review Days
174

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Basic Information

Device Name
MX-7000 MICROXEL
K Number
K111831
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
Bio-Med USA, Inc.
Date Received
June 28, 2011
Decision Date
December 19, 2011
Product Code
ONG
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
ONG Powered Laser Surgical Instrument With MicrobeamFractional Output

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