Cleared Traditional

K092850 - ENDOFLIP

K092850 is an FDA 510(k) clearance for ENDOFLIP, manufactured by Crospon, Ltd.. The device is a Class 2 Gastroenterology & Urology device with product code FFX cleared through the Traditional 510(k) pathway after a 90-day FDA review.

K092850 · Crospon, Ltd. · Gastroenterology & Urology device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Dec 2009
Decision
90d
Days
Class 2
Risk

K092850 is an FDA 510(k) clearance for the ENDOFLIP. Classified as System, Gastrointestinal Motility (electrical) (product code FFX), Class II - Special Controls.

Submitted by Crospon, Ltd. (Bonita Springs, US). The FDA issued a Cleared decision on December 15, 2009 after a review of 90 days - within the typical 510(k) review window.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.1725 - 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.

FDA 510(k) Submission Details - K092850

510(k) Number K092850 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 16, 2009
Decision Date December 15, 2009
Days to Decision 90 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
41d faster than avg
Panel avg: 131d · This submission: 90d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FFX Device Classification - Class 2, Special Controls

Product Code FFX System, Gastrointestinal Motility (electrical)
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.1725
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 - FFX System, Gastrointestinal Motility (electrical)

All 69
Devices cleared under the same product code (FFX) and FDA review panel - the closest regulatory comparables to K092850.
SPHINCTER OF ODDI MANOMETRIC (SOM) SYSTEM
K120524 · Mui Scientific · Jun 2012
ENDO FLIP
K102214 · Crospon, Ltd. · Dec 2010
PHTIP DISPOSABLE ISFET CATHETER
K102801 · E-Cath Co., Ltd. · Oct 2010
MANOSCAN MOTILITY WITH IMPEDANCE VISUALIZATION SYSTEM
K091070 · Sierra Scientific Instruments, Inc. · May 2009
ANORECTAL MANOMETRY SOFTWARE OPTION ARM-1
K082056 · Life-Tech, Inc. · Nov 2008
MODIFICATION TO SOLAR GI
K071094 · Medical Measurement Systems B.V. · Aug 2007
K092850 · ENDOFLIP
Download PDF FDA Summary Crospon, Ltd.