Cleared Traditional

K832807 - PEDIATRIC ILLUMINATING URETERAL

K832807 is the FDA 510(k) clearance for PEDIATRIC ILLUMINATING URETERAL by Van-Tec, Inc.. It is a Class 2 Gastroenterology & Urology device (product code FCW) cleared through the Traditional 510(k) pathway after a 62-day FDA review.

K832807 · Van-Tec, Inc. · Gastroenterology & Urology device
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Oct 1983
Decision
62d
Days
Class 2
Risk

K832807 is an FDA 510(k) clearance for the PEDIATRIC ILLUMINATING URETERAL. Classified as Light Source, Fiberoptic, Routine (product code FCW), Class II - Special Controls.

Submitted by Van-Tec, Inc. (Walker, US). The FDA issued a Cleared decision on October 19, 1983 after a review of 62 days - a notably fast clearance cycle.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.1500 - 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

Submission Details

510(k) Number K832807 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 18, 1983
Decision Date October 19, 1983
Days to Decision 62 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
68d faster than avg
Panel avg: 130d · This submission: 62d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code FCW Light Source, Fiberoptic, Routine
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.1500
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 - FCW Light Source, Fiberoptic, Routine

All 12
Devices cleared under the same product code (FCW) and FDA review panel - the closest regulatory comparables to K832807.
AUTO SUTURE DISPOSABLE LIGHT CABLE
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K852951 · Welch Allyn, Inc. · Aug 1985
PENTAX LH-150F LIGHT SOURCE
K771739 · Pilling Co. · Sep 1977
ADAPTER, FIBER OPTICS HEADLIGHT
K760647 · Pilling Co. · Dec 1976
FLOORSTAND, FIBER OPTIC LIGHT SOURCE
K760176 · V. Mueller O.V. Baxter Healthcare Corp. · Aug 1976