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

CONPHAR PERCUSSION HAMMER(BUCK TYPE)

K Number: K803174 · Decision Dec 30, 1980
Classifications
1
FEI Numbers
70
Registration Numbers
70
Same Product Code
10
Applicant Total
122
Review Days
15

Basic Information

Device Name
CONPHAR PERCUSSION HAMMER(BUCK TYPE)
K Number
K803174
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
882.1700
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
CONPHAR, INC.
Date Received
December 15, 1980
Decision Date
December 30, 1980
Product Code
GWZ
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

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

Product Code Device Name
GWZ Percussor

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K Number Device Name
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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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