CERVEX-BRUSH— 510(k) K890848

Substantially Equivalent

Unimar, Inc.

FDA 510(k) clearance K890848 for CERVEX-BRUSH, Substantially Equivalent on 1989-05-11. Applicant: Unimar, Inc.. Device class: 2.

Clearance details

Applicant: Unimar, Inc.
Product code: Code HHT
Device class: Class 2
Regulation: 21 CFR 884.4530
Advisory panel: Obstetrics/Gynecology
Date received: 1989-02-21
Decision date: 1989-05-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wilton, CT, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HHT

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K141057 — DISPOSABLE CERVICAL BRUSH2015-05-14
K111681 — HISTOBRUSH2012-01-19
K083012 — PAPCONE2009-04-09

More clearances from Unimar, Inc.

K932432 — KRONNER REINFORCING STYLETTE1994-04-12
K920803 — HSG TRAY1992-10-19
K910317 — UNI-SEM(TM)1991-05-01
K904473 — KRONNER MANIPUJECTOR1990-12-14
K895659 — HUI MINI-FLEX1989-12-19

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