Core-M, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
Advertisement
Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K960861 | OMICRON MONITOR, DELTA MONITOR | CBK | 1996-08-19 | View |
| 510(k) | K921978 | BREATH TRACKER(TM) MODEL 1800 CAN-O-GAUGE | CAP | 1992-11-17 | View |
| 510(k) | K892942 | BREATH TRACKER | CAP | 1989-06-23 | View |
No matching devices.
Advertisement