FDA.reportPublic FDA data

510(k) K851724

Device
1410/1 TO 1435/13 VARIOUS PROBES & EXPLORERS
Applicant
ARTIBERIA
510(k) number
K851724
Product code
EKB  
Decision
Substantially Equivalent (SESE)
Decision date
1985-07-02
Date received
1985-04-25
Regulation
872.4565
Classification name
Explorer, Operative
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

Other 510(k) Records For Product Code EKB  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K823914EXPLORER TIPTreace Medical, Inc.1983-01-21
K821780BEACH EXPLORER NO. 23T.G.Pacific Dental Corp.1982-07-06

Legacy Summary#

Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links Follow FDA En Español Home Food Drugs Medical Devices Radiation-Emitting Products Vaccines, Blood & Biologics Animal & Veterinary Cosmetics Tobacco Products FDA Home Medical Devices Databases

FDA Review#

Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links Follow FDA En Español Home Food Drugs Medical Devices Radiation-Emitting Products Vaccines, Blood & Biologics Animal & Veterinary Cosmetics Tobacco Products FDA Home Medical Devices Databases