Cleared Traditional

K110147 - ULTRASIGHTHD C31 WITH IMAGESENSE AND REMOTE VIEWER TELEMEDICINE

K110147 is an FDA 510(k) clearance for ULTRASIGHTHD C31 WITH IMAGESENSE AND RE..., manufactured by Sti Medical Systems, LLC. The device is a Class 2 Obstetrics & Gynecology device with product code HEX cleared through the Traditional 510(k) pathway after a 80-day FDA review.

K110147 · Sti Medical Systems, LLC · Obstetrics & Gynecology device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Apr 2011
Decision
80d
Days
Class 2
Risk

K110147 is an FDA 510(k) clearance for the ULTRASIGHTHD C31 WITH IMAGESENSE AND REMOTE VIEWER TELEMEDICINE. Classified as Colposcope (and Colpomicroscope) (product code HEX), Class II - Special Controls.

Submitted by Sti Medical Systems, LLC (La Jolla, US). The FDA issued a Cleared decision on April 8, 2011 after a review of 80 days - a notably fast clearance cycle.

This device falls under the Obstetrics & Gynecology FDA review panel, regulated under 21 CFR 884.1630 - the FDA obstetrics and gynecology 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 Sti Medical Systems, LLC devices

FDA 510(k) Submission Details - K110147

510(k) Number K110147 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 18, 2011
Decision Date April 08, 2011
Days to Decision 80 days
Submission Type Traditional
Review Panel Obstetrics & Gynecology (OB)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
81d faster than avg
Panel avg: 161d · This submission: 80d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

HEX Device Classification - Class 2, Special Controls

Product Code HEX Colposcope (and Colpomicroscope)
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 884.1630
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 Obstetrics & Gynecology devices follow this clearance model.

Regulatory Peers - HEX Colposcope (and Colpomicroscope)

All 45
Devices cleared under the same product code (HEX) and FDA review panel - the closest regulatory comparables to K110147.
THE GYNOCULAR
K132423 · Gynius AB · Apr 2014
GC-3000E DIGITAL COLPOSCOPE
K122311 · Shenzhen Goldcare Meditech Co., Ltd. · Sep 2013
AL-106, AL-106SA AND AL-106B MEDGYN DIGITAL VIDEO COLPOSCOPE
K122973 · Medgyn Products, Inc. · Jun 2013
DYSIS
K092433 · Forth Photonics Hellas SA · Mar 2011
ULTRASIGHT HD DIGITAL COLPOSCOPY WITH IMAGESENSE TECHNOLOGY
K090324 · Sti Medical Systems · Dec 2010
SEILER COLPOSCOPE, MODELS 935, 955 AND 985
K101141 · Seiler Precision Microscopes · Aug 2010