Cleared Traditional

K900641 - CANNULA, SUCTION UTERINE

K900641 is an FDA 510(k) clearance for CANNULA, manufactured by Williams Specialty Products, Inc.. The device is a Class 2 Obstetrics & Gynecology device with product code HHI cleared through the Traditional 510(k) pathway after a 49-day FDA review.

K900641 · Williams Specialty Products, Inc. · Obstetrics & Gynecology device
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Mar 1990
Decision
49d
Days
Class 2
Risk

K900641 is an FDA 510(k) clearance for the CANNULA, SUCTION UTERINE. Classified as System, Abortion, Vacuum (product code HHI), Class II - Special Controls.

Submitted by Williams Specialty Products, Inc. (Encino, US). The FDA issued a Cleared decision on March 30, 1990 after a review of 49 days - a notably fast clearance cycle.

This device falls under the Obstetrics & Gynecology FDA review panel, regulated under 21 CFR 884.5070 - 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 Williams Specialty Products, Inc. devices

FDA 510(k) Submission Details - K900641

510(k) Number K900641 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 09, 1990
Decision Date March 30, 1990
Days to Decision 49 days
Submission Type Traditional
Review Panel Obstetrics & Gynecology (OB)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
111d faster than avg
Panel avg: 160d · This submission: 49d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

HHI Device Classification - Class 2, Special Controls

Product Code HHI System, Abortion, Vacuum
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 884.5070
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 - HHI System, Abortion, Vacuum

All 7
Devices cleared under the same product code (HHI) and FDA review panel - the closest regulatory comparables to K900641.
BERKELEY V-10 VACUUM CURETTAGE SYSTEM
K030935 · Acmi Corporation · Jun 2003
CYTOPREP
K983181 · Cytoprep Inc. Est. · Nov 1998
MEDI VAC SPECIMEN COLLECTOR AND TRANSPORTER
K931205 · Baxter Healthcare Corp · Mar 1994
SCENTED OR SCENTED DEODORIZED MENSTRUAL PADS
K880734 · Personal Products Co. · Apr 1988
GYNASPYR VACUUM CURETTAGE UNIT
K850312 · Roseburg SA · Feb 1985
UTERINE VACUM ASPIRATING CURRETTE
K802360 · American Hospital Supply Corp. · Oct 1980