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

CONPHAR CAST HEELS

K Number: K803141 · Decision Jan 9, 1981
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
30
Applicant Total
122
Review Days
28

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
CONPHAR CAST HEELS
K Number
K803141
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
888.5940
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Conphar, Inc.
Date Received
December 12, 1980
Decision Date
January 9, 1981
Product Code
LGF
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

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

Product Code Device Name
LGF Component, Cast

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LGF), ordered by most recent decision date.

View all

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. →