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

SILICONE SURGICAL VESSEL LOOPS

K Number: K791370 · Decision Aug 3, 1979
Classifications
1
FEI Numbers
313
Registration Numbers
313
Same Product Code
70
Applicant Total
122
Review Days
10

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Basic Information

Device Name
SILICONE SURGICAL VESSEL LOOPS
K Number
K791370
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
870.4500
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Conphar, Inc.
Date Received
July 24, 1979
Decision Date
August 3, 1979
Product Code
DWS
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
DWS Instruments, Surgical, Cardiovascular

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K Number Device Name
K821825 CONPHAR SILICONE FEEDING TUBE
K821295 OLSEN HEGAR NEEDLE HOLDERS
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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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