Cleared Traditional

K960469 - DETECT CYTOLOGY BRUSH II

K960469 is the FDA 510(k) clearance for DETECT CYTOLOGY BRUSH II by Cook Urological, Inc.. It is a Class 2 Obstetrics & Gynecology device (product code HHT) cleared through the Traditional 510(k) pathway after a 42-day FDA review.

K960469 · Cook Urological, Inc. · Obstetrics & Gynecology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Mar 1996
Decision
42d
Days
Class 2
Risk

K960469 is an FDA 510(k) clearance for the DETECT CYTOLOGY BRUSH II. Classified as Spatula, Cervical, Cytological (product code HHT), Class II - Special Controls.

Submitted by Cook Urological, Inc. (Spencer, US). The FDA issued a Cleared decision on March 14, 1996 after a review of 42 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 Cook Urological, Inc. devices

Submission Details

510(k) Number K960469 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 01, 1996
Decision Date March 14, 1996
Days to Decision 42 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
118d faster than avg
Panel avg: 160d · This submission: 42d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code HHT Spatula, Cervical, Cytological
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 - HHT Spatula, Cervical, Cytological

Devices cleared under the same product code (HHT) and FDA review panel - the closest regulatory comparables to K960469.
exCellerator Cervical Collection Device
K182049 · Excell Company, LLC · Apr 2019
KOTEX SUPER MAXI PADS
K890013 · Kimberly-Clark Corp. · Apr 1989
ENDO CERVICAL CURETTE - EVANS, RANDALL, GUSBERG
K891032 · Zinnanti Surgical Instruments, Inc. · Mar 1989
ORTHO* SPECIMEN COLLECTION CYTOLOGY BRUSH
K875162 · Ortho Diagnostic Systems, Inc. · Jan 1988
ORTHO* SPECIMEN COLLECTION CYTOBRUSH
K871552 · Ortho Diagnostic Systems, Inc. · Jun 1987
CYCLO-BRUSH
K870782 · Medline Industries, Inc. · May 1987