Cleared Traditional

K141523 - ALLY UPS

K141523 is an FDA 510(k) clearance for ALLY UPS, manufactured by CooperSurgical, Inc.. The device is a Class 2 Obstetrics & Gynecology device with product code LKF cleared through the Traditional 510(k) pathway after a 169-day FDA review.

K141523 · CooperSurgical, Inc. · Obstetrics & Gynecology device
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Nov 2014
Decision
169d
Days
Class 2
Risk

K141523 is an FDA 510(k) clearance for the ALLY UPS. Classified as Cannula, Manipulator/injector, Uterine (product code LKF), Class II - Special Controls.

Submitted by CooperSurgical, Inc. (Shelton, US). The FDA issued a Cleared decision on November 25, 2014 after a review of 169 days - an extended review cycle.

This device falls under the Obstetrics & Gynecology FDA review panel, regulated under 21 CFR 884.4530 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Obstetrics & Gynecology review framework, consistent with the majority of Class II 510(k) submissions.

View all CooperSurgical, Inc. devices

FDA 510(k) Submission Details - K141523

510(k) Number K141523 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 09, 2014
Decision Date November 25, 2014
Days to Decision 169 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
9d slower than avg
Panel avg: 160d · This submission: 169d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

LKF Device Classification - Class 2, Special Controls

Product Code LKF Cannula, Manipulator/injector, Uterine
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 884.4530
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 - LKF Cannula, Manipulator/injector, Uterine

All 60
Devices cleared under the same product code (LKF) and FDA review panel - the closest regulatory comparables to K141523.
Air Bubble Based Infuser (ABBI)
K143415 · CooperSurgical, Inc. · Feb 2015
VCARE
K142716 · Conmed Corporation · Feb 2015
MANIPULATOR
K142164 · Gynetech Pty. , Ltd. · Dec 2014
CLEARVIEW TOTAL
K131781 · Clinical Innovations, LLC · May 2014
KRONNER SIDE-KICK UTERINE MANIPULATOR HOLDER
K130758 · Kronner Prototypes, Inc. · Dec 2013
VIKY UP
K122820 · Endocontrol · Jun 2013