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

SMOKE EVACUATION ATTACHMENT 130XXX TBD

K Number: K982309 · Decision Aug 5, 1998
Classifications
1
FEI Numbers
839
Registration Numbers
839
Same Product Code
2251
Applicant Total
90
Review Days
35

Basic Information

Device Name
SMOKE EVACUATION ATTACHMENT 130XXX TBD
K Number
K982309
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
CONMED CORP.
Date Received
July 1, 1998
Decision Date
August 5, 1998
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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