Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K832118Substantially Equivalent

Digident Elektronic Apex Locator

Ora-Muszeripari Szovetkezet, Mchenry IL / Traditional, Substantially Equivalent

K832118 is the FDA 510(k) clearance record for DIGIDENT ELEKTRONIC APEX LOCATOR, cleared for Ora-Muszeripari Szovetkezet on . FDA records list one 510(k) clearance for Ora-Muszeripari Szovetkezet. As of , FDA records show no recalls naming K832118.

Clearance record

Decision date
Received
(88 days to decision)
Review panel
Unknown
Applicant
Ora-Muszeripari Szovetkezet 803 N. Front St. Suite 3, Mchenry IL
Third party review
No