Cleared Traditional

K010056 - UTERINE MANIPULATOR INJECTOR CANNULA, STERILE, MODEL R 57-450

K010056 is an FDA 510(k) clearance for UTERINE MANIPULATOR INJECTOR CANNULA, manufactured by A & A Medical, Inc.. The device is a Class 2 Obstetrics & Gynecology device with product code LKF cleared through the Traditional 510(k) pathway after a 24-day FDA review.

K010056 · A & A Medical, Inc. · Obstetrics & Gynecology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Feb 2001
Decision
24d
Days
Class 2
Risk

K010056 is an FDA 510(k) clearance for the UTERINE MANIPULATOR INJECTOR CANNULA, STERILE, MODEL R 57-450. Classified as Cannula, Manipulator/injector, Uterine (product code LKF), Class II - Special Controls.

Submitted by A & A Medical, Inc. (Alpharetta, US). The FDA issued a Cleared decision on February 1, 2001 after a review of 24 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 A & A Medical, Inc. devices

FDA 510(k) Submission Details - K010056

510(k) Number K010056 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 08, 2001
Decision Date February 01, 2001
Days to Decision 24 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
136d faster than avg
Panel avg: 160d · This submission: 24d
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 K010056.
H/S CATHETER SET (5F), MODEL 61-5005
K020951 · Ackrad Laboratories · Apr 2002
SF SH CATHETER, MODEL R65-945
K013437 · A & A Medical, Inc. · Nov 2001
HSG CATHETER SET, 5F MODEL RGS0947, HSG CATHETER SET, 7F, MODEL R65-948
K013491 · A & A Medical, Inc. · Nov 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