Company ยท US
Echocath, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1993 to 2001. 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 |
|---|---|---|---|
| Mar 20, 2001 | K010482 | ECHOFLOW PORTABLE DOPPLER BLOOD FLOW MEASUREMENT SYSTEM; MODEL PEF-1 Echocath, Inc. | JOP |
| Sep 16, 1999 | K990642 | ECHOFLOW DOPPLER BLOOD VELOCITY METER Echocath, Inc. | JOP |
| Nov 16, 1995 | K932436 | ECHOMARK INTRAUTERINE GUIDING CATHETER Echocath, Inc. | MOV |
| May 4, 1995 | K933417 | ECHOMARK(R) ELECTROPHYSIOLOGY CATHETER Echocath, Inc. | DRF |
| Sep 16, 1993 | K926351 | COLORMARK(TM) VISUALIZATION SYSTEM Echocath, Inc. | IYN |
| Jan 6, 1993 | K922787 | ECHOMARK GUIDEWIRE WITH ULTRASONIC LOCALIZATION Echocath, Inc. | DQX |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||