THE ROBICSEK - PRUITT AORTIC BALLOON OCCLUSION KIT— 510(k) K872090

Name: FDA 510(k) clearance K872090
Creator: U.S. Food and Drug Administration
Published: 1987-10-30

Substantially Equivalent

Ideas For Medicine, Inc.

FDA 510(k) clearance K872090 for THE ROBICSEK - PRUITT AORTIC BALLOON OCCLUSION KIT, Substantially Equivalent on 1987-10-30. Applicant: Ideas For Medicine, Inc.. Device class: 2.

Clearance details

Applicant: Ideas For Medicine, Inc.
Product code: Code DQT
Device class: Class 2
Regulation: 21 CFR 870.1370
Advisory panel: Cardiovascular
Date received: 1987-06-01
Decision date: 1987-10-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Clearwater, FL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code DQT

view all

K983927 — GT1 FLOPPY, GT1 HI-PER FLEX, GT1 LIGHT SUPPORT1999-03-11
K945963 — THE OMNIGUIDE GUIDING CATHETER WITH BALLOON1995-02-08
K910916 — CATHLAB SILICONE OCCLUSION BALLOON CATHETER1991-06-24
K910339 — AVD INTIMAX OCCLUSION CATHETER1991-05-29
K880860 — CORONARY OSTIUM OCCLUDER, CATALOG CODE 320151988-05-26

More clearances from Ideas For Medicine, Inc.

view all

K961883 — VERSA-CATH ARTERIAL CATHETER1997-01-13
K962751 — IDEAS' DUAL PORT1996-09-30
K961716 — VASO-SAFE ARTERIAL EMBOLECTOMY CATHETE1996-09-19
K960715 — PRUITT-INAHARA CAROTID SHUNT 400-40-8F/INAHARA-PRUITT CAROTID SHUNT 500-50-8F1996-09-09
K960422 — PRUITT SAFETY OCCLUSION CATHETER1996-08-07

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