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

CONPHAR STETHSCOPE

K Number: K792112 · Decision Dec 4, 1979
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
153
Applicant Total
122
Review Days
40

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Basic Information

Device Name
CONPHAR STETHSCOPE
K Number
K792112
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1875
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Conphar, Inc.
Date Received
October 25, 1979
Decision Date
December 4, 1979
Product Code
DQD
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
DQD Stethoscope, Electronic

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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. →