Company ยท US
Dynatech/Nevada, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1990 to 1995. Name variants (Inc, Corp, punctuation) are merged.
6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Jan 27, 1995 | K942546 | CUFFLINK NON-INVASIVE BLOOD PRESSURE ANALYZER Dynatech/Nevada, Inc. | DXN |
| Jan 18, 1994 | K935817 | MEDSIM 300 PATIENT SIMULATOR Dynatech/Nevada, Inc. | DRT |
| Nov 23, 1993 | K934254 | IMPULSE 3000 DEFIBRILLATOR ANALYZER Dynatech/Nevada, Inc. | DRL |
| May 17, 1990 | K897074 | MODEL 215M PATIENT SIMULATOR Dynatech/Nevada, Inc. | DSI |
| Apr 26, 1990 | K897029 | MODEL ECG100 SIMULATOR Dynatech/Nevada, Inc. | DPS |
| Mar 15, 1990 | K897096 | MODEL 404A I.V. INFUSION PUMP ANALYZER Dynatech/Nevada, Inc. | FRN |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||