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
FIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.
