Cleared Traditional

K942155 - HMT ENDOSCREEN

K942155 is an FDA 510(k) clearance for HMT ENDOSCREEN, manufactured by Servicetrends, Inc.. The device is a Class 2 Gastroenterology & Urology device with product code FCW cleared through the Traditional 510(k) pathway after a 59-day FDA review.

K942155 · Servicetrends, Inc. · Gastroenterology & Urology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jul 1994
Decision
59d
Days
Class 2
Risk

K942155 is an FDA 510(k) clearance for the HMT ENDOSCREEN, MODEL ESC 501. Classified as Light Source, Fiberoptic, Routine (product code FCW), Class II - Special Controls.

Submitted by Servicetrends, Inc. (Kennesaw, US). The FDA issued a Cleared decision on July 1, 1994 after a review of 59 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 Servicetrends, Inc. devices

FDA 510(k) Submission Details - K942155

510(k) Number K942155 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 03, 1994
Decision Date July 01, 1994
Days to Decision 59 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
71d faster than avg
Panel avg: 130d · This submission: 59d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FCW Device Classification - Class 2, Special Controls

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 13
Devices cleared under the same product code (FCW) and FDA review panel - the closest regulatory comparables to K942155.
STRYKER LED LIGHTSOURCE
K082813 · Stryker Corp. · Dec 2008
ENDOSPOT
K963043 · Corin USA · Sep 1996
WELCH ALLYN HI - LUX ILLUMINATOR
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AUTO SUTURE DISPOSABLE LIGHT CABLE
K934531 · United States Surgical, A Division of Tyco Healthc · May 1994
STORZ S6000 LIGHT SOURCE
K905376 · Storz Instrument Co. · Jan 1991
WELCH ALLYN FIBER OPTIC CABLES VARIOUS MODELS
K852951 · Welch Allyn, Inc. · Aug 1985