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

OLYMPUS PSD-20 ELECTROSURGICAL SYSTEM AND ACCESSORIES

K Number: K970797 · Decision May 28, 1997
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
149
Review Days
85

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Basic Information

Device Name
OLYMPUS PSD-20 ELECTROSURGICAL SYSTEM AND ACCESSORIES
K Number
K970797
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
Olympus America, Inc.
Date Received
March 4, 1997
Decision Date
May 28, 1997
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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