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

NOVATIP FAMILY OF LASER HANDPIECE TIPS

K Number: K971539 · Decision Jun 3, 1997
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
1
Review Days
36

Basic Information

Device Name
NOVATIP FAMILY OF LASER HANDPIECE TIPS
K Number
K971539
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
XANOVA CORP.
Date Received
April 28, 1997
Decision Date
June 3, 1997
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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