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510(k) K851752

Device
9-190,9-200,9-210,9-220 AMPUTATION KNIVES, VARIOUS
Applicant
ARTIBERIA
510(k) number
K851752
Product code
GDN  
Decision
Substantially Equivalent (SESE)
Decision date
1985-06-20
Date received
1985-04-25
Regulation
878.4800
Classification name
Knife, Amputation
Medical specialty
General & Plastic Surgery
Review panel
General & Plastic Surgery
Device class
1
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Contact
GIL M SANCHEZ
Address
4518 Los Ranchitos San Antonio TX US 78233 78233

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Legacy Summary#

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FDA Review#

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