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

RITA MODEL 90 ELECTROSURGICAL ACCESSORY, MODEL 90

K Number: K992693 · Decision Sep 10, 1999
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
11
Review Days
29

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Basic Information

Device Name
RITA MODEL 90 ELECTROSURGICAL ACCESSORY, MODEL 90
K Number
K992693
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Rita Medical Systems
Date Received
August 12, 1999
Decision Date
September 10, 1999
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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K021329 RITA SYSTEM
K003676 RITA MODEL 2500 ELECTROSURGICAL RF GENERATOR
K010060 RITA STARBURST XLI ELECTROSURGICAL DEVICE
K983214 RITA RF GENERATOR AND ACCESSORIES, MODEL 500 SERIES
K993944 RITA MODEL 1500 ELECTROSURGICAL GENERATOR, POWER CORD,FOOTSWITCH,MAIN CABLE, DISPERSIVE ELECTRODE
K983871 RITA MODEL 70 ELECTROSURGICAL PROBE
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