Cleared Special

K112452 - ANGIODYNAMICS SOFT-VU ANGIOGRAPHIC CATHETERS

K112452 is an FDA 510(k) clearance for ANGIODYNAMICS SOFT-VU ANGIOGRAPHIC CATH..., manufactured by AngioDynamics, Inc.. The device is a Class 2 Cardiovascular device with product code DQO cleared through the Special 510(k) pathway after a 218-day FDA review.

K112452 · AngioDynamics, Inc. · Cardiovascular device
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Mar 2012
Decision
218d
Days
Class 2
Risk

K112452 is an FDA 510(k) clearance for the ANGIODYNAMICS SOFT-VU ANGIOGRAPHIC CATHETERS. Classified as Catheter, Intravascular, Diagnostic (product code DQO), Class II - Special Controls.

Submitted by AngioDynamics, Inc. (Latham, US). The FDA issued a Cleared decision on March 30, 2012 after a review of 218 days - an extended review cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.1200 - the FDA cardiovascular device oversight framework. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Iterative device modification. Standard predicate reliance. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

FDA 510(k) Submission Details - K112452

510(k) Number K112452 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 25, 2011
Decision Date March 30, 2012
Days to Decision 218 days
Submission Type Special
Review Panel Cardiovascular (CV)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
93d slower than avg
Panel avg: 125d · This submission: 218d
Pathway characteristics
Modification to existing cleared device.

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 469
Devices cleared under the same product code (DQO) and FDA review panel - the closest regulatory comparables to K112452.
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K113260 · Concentric Medical, Inc. · Mar 2012
SUREFIRE GUIDE SHEATH
K113737 · Surefire Medical, Inc. · Feb 2012
K112452 · ANGIODYNAMICS SOFT-VU ANGIOGRAPHIC CATHETERS
Download PDF AngioDynamics, Inc.