Cleared Traditional

K914984 - E-Z-FLOW ANGIOGRAPHY CATHETERS

K914984 is the FDA 510(k) clearance for E-Z-FLOW ANGIOGRAPHY CATHETERS by E-Z-Em, Inc.. It is a Class 2 Cardiovascular device (product code DQY) cleared through the Traditional 510(k) pathway after a 210-day FDA review.

K914984 · E-Z-Em, Inc. · Cardiovascular device
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May 1992
Decision
210d
Days
Class 2
Risk

K914984 is an FDA 510(k) clearance for the E-Z-FLOW ANGIOGRAPHY CATHETERS, MODIFICATION. Classified as Catheter, Percutaneous (product code DQY), Class II - Special Controls.

Submitted by E-Z-Em, Inc. (Glens Falls, US). The FDA issued a Cleared decision on May 20, 1992 after a review of 210 days - an extended review cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.1250 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Cardiovascular review framework, consistent with the majority of Class II 510(k) submissions.

View all E-Z-Em, Inc. devices

Submission Details

510(k) Number K914984 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 23, 1991
Decision Date May 20, 1992
Days to Decision 210 days
Submission Type Traditional
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
85d slower than avg
Panel avg: 125d · This submission: 210d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code DQY Catheter, Percutaneous
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.1250
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 - DQY Catheter, Percutaneous

All 589
Devices cleared under the same product code (DQY) and FDA review panel - the closest regulatory comparables to K914984.
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VASCULAR CATHETER & WIRE GUIDES W/MEDI-COAT(TM)
K914856 · Cook, Inc. · May 1992
RIGHT ATRIAL CATHETER KITS
K920331 · Akcess Medical Products, Inc. · Apr 1992
TRACKER(R) UNIBODY CATH & TRACKER 25 CATH,MODIFIED
K915521 · Target Therapeutics · Mar 1992