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

ENDOVATIONS(R) .035 PRE-CUT PAPILLATOME

K Number: K934315 · Decision Feb 28, 1994
Classifications
1
FEI Numbers
117
Registration Numbers
117
Same Product Code
187
Applicant Total
37
Review Days
180

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Basic Information

Device Name
ENDOVATIONS(R) .035 PRE-CUT PAPILLATOME
K Number
K934315
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.4300
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Endovations
Date Received
September 1, 1993
Decision Date
February 28, 1994
Product Code
KNS
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
KNS Unit, Electrosurgical, Endoscopic (With Or Without Accessories)

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Other Clearances by Endovations

K Number Device Name
K955413 ENDOVATIONS TRIPLE LUMEN BALLOON DILATATION CATHETER
K942110 INJECT-SNARE
K913841 2 LUMEN ENDOS RETRO CHOLANGIOPANCREA INJEC CATH
K913870 5MM MICROSCISSORS
K911155 OVAL CUP BIOPSY FORCEP
K892218 ENDO-SPONGE
K883093 TRANSENDOSCOPIC ASPIRATION NEEDLE
K873360 ENTERON PERCUTAN. ENDOSCOPIC GASTROSTOMY TRAY-PEG
K875264 WASHING CATHETER
K874062 ENTERON LIVER BIOPSY TRAY
Search all 37 clearances from Endovations →