FDA.reportPublic FDA data

510(k) K851718

Device
930/0 TO 950/6 VARIOUS TYPES OF BONE CURETTES
Applicant
ARTIBERIA
510(k) number
K851718
Product code
EMK  
Decision
Substantially Equivalent (SESE)
Decision date
1985-07-02
Date received
1985-04-25
Regulation
872.4565
Classification name
Curette, Surgical, Dental
Medical specialty
Dental
Review panel
Dental
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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