Atlas FDA

DIAMICS CERCOL CERVICAL SAMPLE COLLECTOR SYSTEM

FDA 510(k) clearance K062433 · decided 2007-03-16

Clearance details

K-number
K062433
Device name
DIAMICS CERCOL CERVICAL SAMPLE COLLECTOR SYSTEM
Applicant
Diamics, Inc.
Decision
Substantially Equivalent
Date received
2006-08-21
Decision date
2007-03-16
Days to decision
207 days
Clearance type
Traditional
Product code
HHT
Device class
2
Regulation number
884.4530
Medical specialty
Obstetrics/Gynecology
Advisory committee
Obstetrics/Gynecology
Location
Novato, CA, US
Third-party review
No
Expedited review
No

+ Add to Predicate Builder ◉ Watch Diamics

Need this as data, not a web page?

Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.

Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
exCellerator Cervical Collection Device (K182049)Excell Company, LLC2019-04-25
Kolplast Cervical Sample Collection Kit (K153128)Kolplast CI SA2017-01-13
DISPOSABLE CERVICAL BRUSH (K141057)Ningbo Hls Medical Products Co., Ltd.2015-05-14
HISTOBRUSH (K111681)Puritan Medical Products Company, LLC2012-01-19
PAPCONE (K083012)Otto Bock Pur Life Science GmbH2009-04-09
BIO NUCLEAR DIAGNOSTICS (ENDO)CERVICAL SAMPLER FOR GYN CYTOLOGY (K081522)Bio Nuclear Diagnostics, Inc.2008-12-05
SOFTPAP CERVICAL CELL COLLECTOR (K072381)Cytocore, Inc.2008-01-30
CERVEX-BRUSH COMBI (K043369)Rovers Medical Devices B.V.2005-02-02
SPATULA, CERVICAL, CYTOLOGICAL, MODEL 22-9107 (K042527)Medical Action Industries, Inc.2004-11-08
DRG SOFTRELEASE (K041018)Doctor'S Research Group, Inc.2004-10-18
INPATH E2 COLLECTOR (K013258)Molecular Diagnostics2002-05-31
ROVERS SPATULA (K002520)Rovers Medical Devices B.V.2000-11-13

Recalls involving this device

No recalls on record reference this clearance.