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

CONPHAR BLOOD PRESSURE CUFFS

K Number: K792108 · Decision Dec 4, 1979
Classifications
1
FEI Numbers
175
Registration Numbers
175
Same Product Code
192
Applicant Total
122
Review Days
40

Basic Information

Device Name
CONPHAR BLOOD PRESSURE CUFFS
K Number
K792108
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1120
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
CONPHAR, INC.
Date Received
October 25, 1979
Decision Date
December 4, 1979
Product Code
DXQ
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
DXQ Blood Pressure Cuff

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K Number Device Name
K821825 CONPHAR SILICONE FEEDING TUBE
K821289 MAYO-HEGAR NEEDLE HOLDER
K821295 OLSEN HEGAR NEEDLE HOLDERS
K821354 CONPHAR MAYO HEGAR NEEDLE HOLDER
K821275 MAYO SCISSOR STRAIGHT 5 1/2
K821276 MAYO SCISSOR CURYED 5 1/2
K821273 MAYO SCISSOR STRAIGHT 6 3/4
K821285 SPLINTER FORCEPS 4 1/2
K821284 ADSON FORCEPS 4 3/4
K821292 TONSIL SCISSORS 7
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