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

ROCHESTER PEAN FORCEPS

K Number: K821248 · Decision May 28, 1982
Classifications
1
FEI Numbers
444
Registration Numbers
445
Same Product Code
103
Applicant Total
122
Review Days
25

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Basic Information

Device Name
ROCHESTER PEAN FORCEPS
K Number
K821248
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Conphar, Inc.
Date Received
May 3, 1982
Decision Date
May 28, 1982
Product Code
GEN
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
GEN Forceps, General & Plastic Surgery

Similar 510(k) Clearances

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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
K821294 TONSIL SCISSORS STRAIGHT 5 1/2
Search all 122 clearances from Conphar, Inc. →