Cleared Traditional

K851144 - URETERAL DILATION SET

K851144 is an FDA 510(k) clearance for URETERAL DILATION SET, manufactured by Van-Tec, Inc.. The device is a Class 2 Gastroenterology & Urology device with product code EZN cleared through the Traditional 510(k) pathway after a 19-day FDA review.

K851144 · Van-Tec, Inc. · Gastroenterology & Urology device
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Apr 1985
Decision
19d
Days
Class 2
Risk

K851144 is an FDA 510(k) clearance for the URETERAL DILATION SET. Classified as Dilator, Catheter, Ureteral (product code EZN), Class II - Special Controls.

Submitted by Van-Tec, Inc. (Spencer, US). The FDA issued a Cleared decision on April 9, 1985 after a review of 19 days - a notably fast clearance cycle.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.5470 - the FDA gastroenterology and urology device 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 Van-Tec, Inc. devices

FDA 510(k) Submission Details - K851144

510(k) Number K851144 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 21, 1985
Decision Date April 09, 1985
Days to Decision 19 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
112d faster than avg
Panel avg: 131d · This submission: 19d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

EZN Device Classification - Class 2, Special Controls

Product Code EZN Dilator, Catheter, Ureteral
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.5470
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 Gastroenterology & Urology devices follow this clearance model.

Regulatory Peers - EZN Dilator, Catheter, Ureteral

All 51
Devices cleared under the same product code (EZN) and FDA review panel - the closest regulatory comparables to K851144.
URETERAL DILATOR
K852324 · American Edwards Laboratories · Aug 1985
URETERAL DILATOR/SHEATH SET
K852793 · American Edwards Laboratories · Aug 1985
OLBERT CATHETER SYS FOR URETERAL DILATION
K851463 · Meadox Surgimed, Inc. · May 1985
MENTOR PERCUTANEOUS RENAL DILATOR SET
K850355 · Mentor Corp. · Mar 1985
DIAFLEX NEPHROSTOMY BALLOON DILATOR
K842206 · American Edwards Laboratories · Oct 1984
DILATOR/SHEATH SET
K842632 · American Edwards Laboratories · Oct 1984