Unimar, Inc.
FDA 510(k) & PMA Approved Devices — 10 products
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Total Devices10
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K932432 | KRONNER REINFORCING STYLETTE | LKF | 1994-04-12 | View |
| 510(k) | K920803 | HSG TRAY | HIB | 1992-10-19 | View |
| 510(k) | K910317 | UNI-SEM(TM) | MFD | 1991-05-01 | View |
| 510(k) | K904473 | KRONNER MANIPUJECTOR | HES | 1990-12-14 | View |
| 510(k) | K895659 | HUI MINI-FLEX | HIG | 1989-12-19 | View |
| 510(k) | K895403 | ASPIRETTE ENDOCERVICAL ASPIRATOR | HFC | 1989-11-29 | View |
| 510(k) | K894264 | KDF-2.3 | HDR | 1989-08-15 | View |
| 510(k) | K890848 | CERVEX-BRUSH | HHT | 1989-05-11 | View |
| 510(k) | K854415 | ENDOMETRIAL PIPELLE | HHK | 1986-03-13 | View |
| 510(k) | K810291 | STERILE/DISPOSABLE HSG TRAY | EYY | 1981-03-18 | View |
No matching devices.
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