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

DYONICS ELECTROBLADE

K Number: K994365 · Decision Mar 13, 2000
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
529
Review Days
77

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Basic Information

Device Name
DYONICS ELECTROBLADE
K Number
K994365
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Smith & Nephew, Inc.
Date Received
December 27, 1999
Decision Date
March 13, 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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