# Echocath, Inc.

- Location (FDA's records): Princeton, NJ
- FDA decisions: 6 (1993–2001): 6 510(k) clearances
- Product codes: JOP (2), IYN (1), MOV (1), DRF (1), DQX (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 3 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Ultramed, Inc.: 1 (https://510kreport.com/company/ultramed)
- Zertl Medical, Inc.: 1 (https://510kreport.com/company/zertl-medical)

## Firms that cite its devices most
- Biosonix, Ltd.: 1 (https://510kreport.com/company/biosonix)
- Nuvue Therapeutics, Inc.: 1 (https://510kreport.com/company/nuvue-therapeutics)
- Ultraguide, Ltd.: 1 (https://510kreport.com/company/ultraguide)

## Its most-cited devices
- K926351: Colormark (TM) Visualization System (1993), cited by 2
- K990642: Echoflow Doppler Blood Velocity Meter (1999), cited by 1

## Recent decisions
- K010482: Echoflow Portable Doppler Blood Flow Measurement System; Model Pef-1 (Mar 20, 2001)
- K990642: Echoflow Doppler Blood Velocity Meter (Sep 16, 1999)
- K932436: Echomark Intrauterine Guiding Catheter (Nov 16, 1995)
- K933417: Echomark (R) Electrophysiology Catheter (May 4, 1995)
- K926351: Colormark (TM) Visualization System (Sep 16, 1993)
- K922787: Echomark Guidewire with Ultrasonic Localization (Jan 6, 1993)

Source page: https://510kreport.com/company/echocath