FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

CONPHAR O.R. HEAD COVER-STERILE

K Number: K792106 · Decision Nov 5, 1979
Classifications
1
FEI Numbers
3
Registration Numbers
3
Same Product Code
3
Applicant Total
122
Review Days
11

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Basic Information

Device Name
CONPHAR O.R. HEAD COVER-STERILE
K Number
K792106
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.3250
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Conphar, Inc.
Date Received
October 25, 1979
Decision Date
November 5, 1979
Product Code
FYI
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
FYI Appliance, Facial Fracture, External

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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
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