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

BALLOON ELECTROSURGICAL PROBES AND DEVICES

K Number: K943014 · Decision Mar 11, 1996
Classifications
1
FEI Numbers
839
Registration Numbers
839
Same Product Code
2251
Applicant Total
11
Review Days
626

Basic Information

Device Name
BALLOON ELECTROSURGICAL PROBES AND DEVICES
K Number
K943014
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
XIMED MEDICAL SYSTEMS
Date Received
June 24, 1994
Decision Date
March 11, 1996
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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