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

CONPHAR NELATON CATHETER-STERILE

K Number: K791264 · Decision Aug 3, 1979
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
237
Applicant Total
122
Review Days
28

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Basic Information

Device Name
CONPHAR NELATON CATHETER-STERILE
K Number
K791264
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5130
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Conphar, Inc.
Date Received
July 6, 1979
Decision Date
August 3, 1979
Product Code
KOD
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
KOD Catheter, Urological

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Other Clearances by Conphar, Inc.

K Number Device Name
K821825 CONPHAR SILICONE FEEDING TUBE
K821295 OLSEN HEGAR NEEDLE HOLDERS
K821354 CONPHAR MAYO HEGAR NEEDLE HOLDER
K821289 MAYO-HEGAR NEEDLE HOLDER
K821298 BACKHAUS CLAMP, 3 1/2
K821285 SPLINTER FORCEPS 4 1/2
K821276 MAYO SCISSOR CURYED 5 1/2
K821275 MAYO SCISSOR STRAIGHT 5 1/2
K821284 ADSON FORCEPS 4 3/4
K821248 ROCHESTER PEAN FORCEPS
Search all 122 clearances from Conphar, Inc. →