Cleared Traditional

K905297 - DIAVENTIONAL CATHETER

K905297 is an FDA 510(k) clearance for DIAVENTIONAL CATHETER, manufactured by Cordis Corp.. The device is a Class 2 Cardiovascular device with product code DQO cleared through the Traditional 510(k) pathway after a 66-day FDA review.

K905297 · Cordis Corp. · Cardiovascular device
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Feb 1991
Decision
66d
Days
Class 2
Risk

K905297 is an FDA 510(k) clearance for the DIAVENTIONAL CATHETER. Classified as Catheter, Intravascular, Diagnostic (product code DQO), Class II - Special Controls.

Submitted by Cordis Corp. (Miami Lakes, US). The FDA issued a Cleared decision on February 1, 1991 after a review of 66 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.1200 - the FDA cardiovascular device oversight framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Cordis Corp. devices

FDA 510(k) Submission Details - K905297

510(k) Number K905297 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 27, 1990
Decision Date February 01, 1991
Days to Decision 66 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
59d faster than avg
Panel avg: 125d · This submission: 66d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DQO Device Classification - Class 2, Special Controls

Product Code DQO Catheter, Intravascular, Diagnostic
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.1200
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Cardiovascular devices follow this clearance model.

Regulatory Peers - DQO Catheter, Intravascular, Diagnostic

All 320
Devices cleared under the same product code (DQO) and FDA review panel - the closest regulatory comparables to K905297.
ACS ANGIOSCOPIC CATHETER
K905715 · Advanced Cardiovascular Systems, Inc. · Mar 1991
SCIMD 7 FR. TRIGUIDE GUIDING CATHETER
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TMP LEFT ATRIAL PRESSURE CATH CAT.# 100-00X-000
K904491 · Lifestream Int'L, Inc. · Feb 1991
USCI SATIN FINISH SOFT TIP ANGIOGRAPHIC CATHETER
K905727 · C.R. Bard, Inc. · Feb 1991
HOLLOW LUMEN NEEDLE, PART NUMBER: MX920
K903199 · Medex, Inc. · Dec 1990
MEWISSEN CATHETER
K904788 · Boston Scientific Corp · Dec 1990