DOPPLER NEEDLE AND FLOW MONITOR— 510(k) K903625

Name: FDA 510(k) clearance K903625
Creator: U.S. Food and Drug Administration
Published: 1990-11-07

Substantially Equivalent

Peripheral Systems Group

FDA 510(k) clearance K903625 for DOPPLER NEEDLE AND FLOW MONITOR, Substantially Equivalent on 1990-11-07. Applicant: Peripheral Systems Group. Device class: 2.

Clearance details

Applicant: Peripheral Systems Group
Product code: Code DPW
Device class: Class 2
Regulation: 21 CFR 870.2100
Advisory panel: Cardiovascular
Date received: 1990-08-10
Decision date: 1990-11-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mountain View, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code DPW

view all

K260700 — BlueDop Vascular Expert2026-07-08
K252810 — FloPatch FP1202026-04-24
K251904 — VascuChek Kit, VascuChek Transceiver, VascuChek Clinical Probe, VascuChek Speaker Dock (VC-KIT-02, VC-TRX-02, VC-CP-01, VC-SD-01) +1 more2025-11-20
K251114 — FloPatch FP1202025-06-20
K243852 — Elfor-L2025-04-14

More clearances from Peripheral Systems Group

view all

K940804 — SMARTNEEDLE VASCULAR ACCESS SYSTEM, MODIFICATION1994-06-10
K934433 — VANTAGE DIALTAION CATHETER1993-12-09
K932777 — SMARTNEEDLE(R) OVER-THE-NEEDLE CATHETER1993-10-07
K931327 — PSG DIRECTIONAL HYDROPHILIC GUIDE WIRE1993-07-14
K915554 — HI-TORQUE SPORT-T(TM) GUIDE WIRE1993-02-09

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