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

ELECTROSURGERY ANALYZER RF302

K Number: K893659 · Decision Jul 14, 1989
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
37
Review Days
60

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Basic Information

Device Name
ELECTROSURGERY ANALYZER RF302
K Number
K893659
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Bio-Tek Instruments, Inc.
Date Received
May 15, 1989
Decision Date
July 14, 1989
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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