VENTRICULAR CATHETER BLOOD FLOW MONITORING PROBE KIT AND VENTRAFLO BLOOD FLOW MONITORING PROBE KIT— 510(k) K962700

Name: FDA 510(k) clearance K962700
Creator: U.S. Food and Drug Administration
Published: 1997-04-09

Substantially Equivalent

Vasamedics, LLC

FDA 510(k) clearance K962700 for VENTRICULAR CATHETER BLOOD FLOW MONITORING PROBE KIT AND VENTRAFLO BLOOD FLOW MONITORING PROBE KIT, Substantially Equivalent on 1997-04-09. Applicant: Vasamedics, LLC. Device class: 2.

Clearance details

Applicant: Vasamedics, LLC
Product code: Code DPT
Device class: Class 2
Regulation: 21 CFR 870.2120
Advisory panel: Cardiovascular
Date received: 1996-07-12
Decision date: 1997-04-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Saint Paul, MN, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code DPT

view all

K233076 — Laser Speckle Imaging System (RFLSI CZW)2024-05-28
K163339 — SPECTRALMD DEEPVIEW WOUND IMAGING SYSTEM 2.02017-08-17
K152749 — moorLDI2-IR Infrared laser Doppler imager, moorLDI2-HIR High Resolution Infrared laser Doppler imager, moorLDI2-VR Visible Red laser Doppler imager2016-05-12
K142932 — Deltex Medical KDP72 Doppler Probe2015-01-22
K132730 — BIO-PROBE DISPOSABLE INSERT WITH; BALANCE BIOSURFACE, CARMEDA BIOACTIVE SURFACE, TRILLIUM BIOSURFACE2014-05-30

More clearances from Vasamedics, LLC

view all

K961368 — TRIMFLO PARENCHYMAL BLOOD FLOW MONITORING PROBE KIT1996-10-11
K951832 — LASERFLO BLOOD PERFUSION SINGLE USE PROBES MODELS SUP-440, SUPR-434 SUP-4331996-03-21
K951486 — MODEL PV2000 VASCULAR MICROLABORATORY1995-06-29
K912446 — MODIF. LASERFLO BLOOD PERFUSION MONITOR MODEL BPM21991-12-12
K911763 — LASERFLO(R) BLOOD PERFUSION MONITOR (MODEL BPM2)1991-08-13

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