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

CONMED TROGARD

K Number: K934799 · Decision Dec 21, 1994
Classifications
1
FEI Numbers
153
Registration Numbers
153
Same Product Code
337
Applicant Total
92
Review Days
440

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Basic Information

Device Name
CONMED TROGARD
K Number
K934799
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1720
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Conmedcorp
Date Received
October 7, 1993
Decision Date
December 21, 1994
Product Code
HET
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HET Laparoscope, Gynecologic (And Accessories)

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Other Clearances by Conmedcorp

K Number Device Name
K101534 CONMED ALTRUS THERMAL TISSUE FUSION SYSTEM
K061021 ENTAKE STANDARD AND SAFETY PEG SYSTEM
K050992 CONMED IRRIGATION NOZZLE
K050777 PROFORMA HF 4.5 CANNULA, MODEL 050906, 050907
K050304 FX WIRE ADVANCED MEASUREMENT GUIDEWIRE
K041953 VERSASTIM, PERFOAMAX, SURGI-STIM, FASTSTART
K021079 ABCSNARE ELECTROSURGICAL PROBE FOR FLEXIBLE ENDOSCOPES, MODEL 1336XX
K021299 CONMED HEATWAVE HAND-CONTROLLED ELETRODE
K020135 CONMED SYSTEM 2000 ELECTROSURGICAL GENERATOR, REF: 60-8002; CONMED ESU CART, REF: 60-6120
K020186 CONMED SYSTEM 5000 ESU
Search all 92 clearances from Conmedcorp →