Company ยท US
Koven and Assoc., Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1989 to 1993. Name variants (Inc, Corp, punctuation) are merged.
8510(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 29, 1993 | K922669 | MULTIDOP MODEL HD-2020 BI-DIRECTIONAL BLOOD FLOW Koven and Assoc., Inc. | DPW |
| Jan 22, 1993 | K920333 | SMARTDOP 20 BI-DIRECTIONAL BLOOD FLOW DETECTOR Koven and Assoc., Inc. | DPW |
| Dec 10, 1992 | K915550 | MINI DOPPLER II ULTRASOUND BLOOD FLOW DETECTOR Koven and Assoc., Inc. | DPW |
| Mar 27, 1992 | K913595 | DS-240 AMBULATORY BLOOD PRESSURE MONITORING SYSTEM Koven and Assoc., Inc. | DXN |
| Dec 23, 1991 | K912409 | MODEL HD-207 BIDIRECTIONAL VELOCITY METER Koven and Assoc., Inc. | JOP |
| Feb 26, 1991 | K903026 | ES-1000SP II SMART DOP Koven and Assoc., Inc. | DPW |
| Oct 27, 1989 | K894892 | HD-2200 PNEUMO-DOP VASCULAR TESTING SYSTEM Koven and Assoc., Inc. | DSB |
| Jul 28, 1989 | K892707 | DVM-4200 BLOOD FLOWMETER Koven and Assoc., Inc. | DPW |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||