Cleared Traditional

K960230 - SNARE

K960230 is an FDA 510(k) clearance for SNARE, manufactured by Lighthouse Medical, Inc.. The device is a Class 2 Gastroenterology & Urology device with product code FDI cleared through the Traditional 510(k) pathway after a 196-day FDA review.

K960230 · Lighthouse Medical, Inc. · Gastroenterology & Urology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jul 1996
Decision
196d
Days
Class 2
Risk

K960230 is an FDA 510(k) clearance for the SNARE. Classified as Snare, Flexible (product code FDI), Class II - Special Controls.

Submitted by Lighthouse Medical, Inc. (Waltham, US). The FDA issued a Cleared decision on July 31, 1996 after a review of 196 days - an extended review cycle.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.4300 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Gastroenterology & Urology review framework, consistent with the majority of Class II 510(k) submissions.

View all Lighthouse Medical, Inc. devices

FDA 510(k) Submission Details - K960230

510(k) Number K960230 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 17, 1996
Decision Date July 31, 1996
Days to Decision 196 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
66d slower than avg
Panel avg: 130d · This submission: 196d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FDI Device Classification - Class 2, Special Controls

Product Code FDI Snare, Flexible
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.4300
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 - FDI Snare, Flexible

All 44
Devices cleared under the same product code (FDI) and FDA review panel - the closest regulatory comparables to K960230.
INJECTOR NEEDLE/SNARE
K040961 · United States Endoscopy Group, Inc. · Jul 2004
MILL-ROSE DISPOSABLE POLYPECTOMY SNARE
K971275 · Mill-Rose Laboratory · May 1997
IRRIGATION/ASPIRATION POLYPECTOMY
K970356 · United States Endoscopy Group, Inc. · Mar 1997
OLYMPUS SD SERIES SNARES
K955650 · Olympus America, Inc. · Mar 1996
MILL-ROSE ROTATABLE POLYPECTOMY SNARE
K951600 · Mill-Rose Laboratory · Dec 1995
SNARE, FLEXIBLE, ELECTROSURGICAL CUTTING & COAGULATION DEVICE & ACCESSORIES
K950496 · Boston Scientific Corp · Mar 1995