ECHOFLOW DOPPLER BLOOD VELOCITY METER— 510(k) K990642

Name: FDA 510(k) clearance K990642
Creator: U.S. Food and Drug Administration
Published: 1999-09-16

Substantially Equivalent

Echocath, Inc.

FDA 510(k) clearance K990642 for ECHOFLOW DOPPLER BLOOD VELOCITY METER, Substantially Equivalent on 1999-09-16. Applicant: Echocath, Inc.. Device class: 2.

Clearance details

Applicant: Echocath, Inc.
Product code: Code JOP
Device class: Class 2
Regulation: 21 CFR 870.2880
Advisory panel: Cardiovascular
Date received: 1999-02-26
Decision date: 1999-09-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Monmouth Junction, NJ, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code JOP

view all

K242662 — Falcon/Xpress (Falcon/Xpress)2024-12-18
K233976 — VasoGuard (V10, V8, V6, V4, V2)2024-07-19
K153762 — Smartdop XT62016-05-25
K131623 — SMARTDOP XT2014-01-17
K131860 — VASCULAB VL4000 PHOTOPLETHYSMOGRAPH WITH PULSE VOLUME RECORDING2013-09-27

More clearances from Echocath, Inc.

view all

K010482 — ECHOFLOW PORTABLE DOPPLER BLOOD FLOW MEASUREMENT SYSTEM; MODEL PEF-12001-03-20
K932436 — ECHOMARK INTRAUTERINE GUIDING CATHETER1995-11-16
K933417 — ECHOMARK(R) ELECTROPHYSIOLOGY CATHETER1995-05-04
K926351 — COLORMARK(TM) VISUALIZATION SYSTEM1993-09-16
K922787 — ECHOMARK GUIDEWIRE WITH ULTRASONIC LOCALIZATION1993-01-06

Data sourced from openFDA. This site is unofficial and independent of the FDA.