Cleared Traditional

K001115 - ULTRA CATHETER SET

K001115 is an FDA 510(k) clearance for ULTRA CATHETER SET, manufactured by Lyco Enterprises, Inc.. The device is a Class 2 Obstetrics & Gynecology device with product code LKF cleared through the Traditional 510(k) pathway after a 41-day FDA review.

K001115 · Lyco Enterprises, Inc. · Obstetrics & Gynecology device
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May 2000
Decision
41d
Days
Class 2
Risk

K001115 is an FDA 510(k) clearance for the ULTRA CATHETER SET. Classified as Cannula, Manipulator/injector, Uterine (product code LKF), Class II - Special Controls.

Submitted by Lyco Enterprises, Inc. (El Paso, US). The FDA issued a Cleared decision on May 17, 2000 after a review of 41 days - a notably fast clearance 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: 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 Lyco Enterprises, Inc. devices

FDA 510(k) Submission Details - K001115

510(k) Number K001115 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 06, 2000
Decision Date May 17, 2000
Days to Decision 41 days
Submission Type Traditional
Review Panel Obstetrics & Gynecology (OB)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
119d faster than avg
Panel avg: 160d · This submission: 41d
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 61
Devices cleared under the same product code (LKF) and FDA review panel - the closest regulatory comparables to K001115.
HSG CATHETER SET, 5F MODEL RGS0947, HSG CATHETER SET, 7F, MODEL R65-948
K013491 · A & A Medical, Inc. · Nov 2001
UTERINE MANIPULATOR INJECTOR CANNULA, STERILE, MODEL R 57-450
K010056 · A & A Medical, Inc. · Feb 2001
PBN HYSTERO-SALPINGOGRAPHY CATHETER SET
K000433 · Medical Device Technologies, Inc. · Jun 2000
UTERINE MANIPULATOR/INJECTOR
K974357 · Catheter Research, Inc. · Feb 1998
INTRAUTERINE INSEMINATION AND SONOHYSTEROGRAPHY CATHETER
K970492 · Ackrad Laboratories · Apr 1997
H/S CATHETER SET(61-3005, 61-3007, 61-3605, 61-3607)
K961752 · Ackrad Laboratories · Aug 1996