OSADA ENDEX
FDA 510(k) clearance K904742 · decided 1990-12-17
Clearance details
- K-number
- K904742
- Device name
- OSADA ENDEX
- Applicant
- Osada Electric Co., Ltd.
- Decision
- Substantially Equivalent
- Date received
- 1990-10-18
- Decision date
- 1990-12-17
- Days to decision
- 60 days
- Clearance type
- Traditional
- Product code
- LQY
- Device class
- U
- Medical specialty
- Unknown
- Advisory committee
- Unknown
- Location
- Los Angeles, CA, US
- Third-party review
- No
- Expedited review
- No
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| Root Apex Locator (K212178) | Foshan Coxo Medical Instrument Co., Ltd. | 2022-07-20 |
| EQ-PEX (K210789) | Meta Systems Co., Ltd. | 2021-10-20 |
| BOMEDENT Apex locator, WISMY Apex locator (K203836) | Changzhou Bomedent Medical Technology Co.,Ltd | 2021-03-30 |
| Propex IQ Apex Locator (K191806) | Dentsply Sirona | 2019-10-03 |
| Apex Locator, DPEX III (K181087) | Guilin Woodpecker Medical Instrument Co., Ltd. | 2018-12-18 |
| Dr’s Finder NEO (K171867) | Good Doctors Co., Ltd. | 2018-03-30 |
| Dr's Finder (K151274) | Good Doctors Co., Ltd. | 2016-02-04 |
Recalls involving this device
No recalls on record reference this clearance.