DIGIDENT ELEKTRONIC APEX LOCATOR
FDA 510(k) clearance K832118 · decided 1983-09-26
Clearance details
- K-number
- K832118
- Device name
- DIGIDENT ELEKTRONIC APEX LOCATOR
- Applicant
- Ora-Muszeripari Szovetkezet
- Decision
- Substantially Equivalent
- Date received
- 1983-06-30
- Decision date
- 1983-09-26
- Days to decision
- 88 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Ora-Muszeripari Szovetkezet
The Builder collects up to 8 candidate devices side by side with yours, then exports the substantial-equivalence comparison scaffold. How it works
Need this as data, not a web page?
Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.
Recalls involving this device
No recalls on record reference this clearance.