Atlas FDA

THE OMNIGUIDE GUIDING CATHETER WITH BALLOON

FDA 510(k) clearance K945963 · decided 1995-02-08

Clearance details

K-number
K945963
Device name
THE OMNIGUIDE GUIDING CATHETER WITH BALLOON
Applicant
Micro Interventional Systems, Inc.
Decision
Substantially Equivalent
Date received
1994-12-07
Decision date
1995-02-08
Days to decision
63 days
Clearance type
Traditional
Product code
DQT
Device class
2
Regulation number
870.1370
Medical specialty
Cardiovascular
Advisory committee
Cardiovascular
Location
Sunnyvale, CA, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
GT1 FLOPPY, GT1 HI-PER FLEX, GT1 LIGHT SUPPORT (K983927)Arterial Vascular Engineering, Inc.1999-03-11
CATHLAB SILICONE OCCLUSION BALLOON CATHETER (K910916)Cathlab Corp.1991-06-24
AVD INTIMAX OCCLUSION CATHETER (K910339)Applied Vascular Devices, Inc.1991-05-29
CORONARY OSTIUM OCCLUDER, CATALOG CODE 32015 (K880860)Dlp, Inc.1988-05-26
MODIFIED PRUITT IRRIGATION & OCCLUSION CATHETER (K880231)Ideas For Medicine, Inc.1988-05-25
THE ROBICSEK - PRUITT AORTIC BALLOON OCCLUSION KIT (K872090)Ideas For Medicine, Inc.1987-10-30
PERFUSION CATHETER (K872790)Bd Becton Dickinson Vacutainer Systems Preanalytic1987-09-15
MODIFIED INFO INSERTS FOR PRUITT IRRI.-OCCLU. CATH (K872154)Ideas For Medicine, Inc.1987-08-03
URESIL OCCLUSION BALLOON CATHETER (K863559)Uresil Corp.1986-10-10
OCCLUSION & OCCLUSION-IRRIGATION (K844918)Clincal Instruments Corp.1985-08-05
ACS SOF-T GUIDE WIREE (K840795)Advanced Cardiovascular Systems, Inc.1984-07-02

Recalls involving this device

No recalls on record reference this clearance.