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

VARPR 3.5MM 90 SUCTION ELECTRODE FOR USE WITH VAPR SYSTEM

K Number: K002422 · Decision Aug 31, 2000
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
30
Review Days
23

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Basic Information

Device Name
VARPR 3.5MM 90 SUCTION ELECTRODE FOR USE WITH VAPR SYSTEM
K Number
K002422
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Mitek Products
Date Received
August 8, 2000
Decision Date
August 31, 2000
Product Code
GEI
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
GEI Electrosurgical, Cutting & Coagulation & Accessories

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