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

ELECTROSURGICAL PENCIL WITH PTFE COATED & UNCOATED ELECTRODE TIPS

K Number: K081647 · Decision Aug 12, 2008
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
6
Review Days
61

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Basic Information

Device Name
ELECTROSURGICAL PENCIL WITH PTFE COATED & UNCOATED ELECTRODE TIPS
K Number
K081647
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
Xodus Medical, Inc.
Date Received
June 12, 2008
Decision Date
August 12, 2008
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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K053321 LIGHT GUARD LIGHT HANDLE AND LIGHT HANDLE COVER