Cleared Traditional

K896690 - MODIFIED ANGIOGRAPHIC CATHETER

K896690 is an FDA 510(k) clearance for MODIFIED ANGIOGRAPHIC CATHETER, manufactured by Novoste Corp.. The device is a Class 2 Cardiovascular device with product code DQO cleared through the Traditional 510(k) pathway after a 57-day FDA review.

K896690 · Novoste Corp. · Cardiovascular device
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Jan 1990
Decision
57d
Days
Class 2
Risk

K896690 is an FDA 510(k) clearance for the MODIFIED ANGIOGRAPHIC CATHETER. Classified as Catheter, Intravascular, Diagnostic (product code DQO), Class II - Special Controls.

Submitted by Novoste Corp. (Aguadilla, US). The FDA issued a Cleared decision on January 24, 1990 after a review of 57 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 Novoste Corp. devices

FDA 510(k) Submission Details - K896690

510(k) Number K896690 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 28, 1989
Decision Date January 24, 1990
Days to Decision 57 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
68d faster than avg
Panel avg: 125d · This submission: 57d
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 413
Devices cleared under the same product code (DQO) and FDA review panel - the closest regulatory comparables to K896690.
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K896741 · Schneider Intl., Ltd. · Feb 1990
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MULTILUMEN CENTRAL VENOUS CATHETER
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BIOCHEM 3100 OXIMETER
K893877 · Biochem International, Inc. · Dec 1989