CERVEX-BRUSH PAP KIT— 510(k) K941472

Unknown

Rovers Diagnostic Devices

FDA 510(k) clearance K941472 for CERVEX-BRUSH PAP KIT, Unknown on 1995-02-28. Applicant: Rovers Diagnostic Devices. Device class: 2.

Clearance details

Applicant: Rovers Diagnostic Devices
Product code: Code HHT
Device class: Class 2
Regulation: 21 CFR 884.4530
Advisory panel: Obstetrics/Gynecology
Date received: 1994-03-28
Decision date: 1995-02-28
Decision: Unknown
Clearance type: Traditional
Location: Nyack, NY, US

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Recent devices under product code HHT

K182049 — exCellerator Cervical Collection Device2019-04-25
K153128 — Kolplast Cervical Sample Collection Kit2017-01-13
K141057 — DISPOSABLE CERVICAL BRUSH2015-05-14
K111681 — HISTOBRUSH2012-01-19
K083012 — PAPCONE2009-04-09

More clearances from Rovers Diagnostic Devices

K942843 — CERVEX-BRUSH(R), STERILE, SPATULA, CERVICAL, CYTOLOGY1994-12-08
K942144 — URETHRA-BRUSH1994-06-27

Data sourced from openFDA. This site is unofficial and independent of the FDA.