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510(k) K882628

ENDO C BRUSH by Milex Products, Inc. — Product Code HHT

K882628 is an FDA 510(k) premarket notification submitted by Milex Products, Inc. for the device "ENDO C BRUSH". The FDA issued a decision of Substantially Equivalent on July 25, 1988. The device falls under product code HHT (Spatula, Cervical, Cytological), a Class II device regulated under 21 CFR 884.4530. Milex Products, Inc. has at least 7 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 25, 1988
Date Received
June 27, 1988
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Spatula, Cervical, Cytological
Device Class
Class II
Regulation Number
884.4530
Review Panel
OB
Submission Type

Other clearances by Milex Products, Inc.

  • K001545 — PIPET CURET (June 15, 2000)
  • K904774 — INGLAT-O-BALL (December 7, 1990)
  • K904026 — INFLAT-O-BALL (October 10, 1990)
  • K900903 — KOPANS HOOKWIRE LESION LOCALIZATION NEEDLE (May 3, 1990)
  • K862410 — MILEX KEGEL PERINEAL EXERCISER (July 31, 1986)
  • K861385 — MILEX BARTHOLIN GLAND CATHETER (June 16, 1986)
  • K760264 — CURETTE, PROPOSED TIS-U-TRAP, METAL (October 6, 1976)

Other clearances for product code HHT

  • K182049 — exCellerator Cervical Collection Device (April 25, 2019)
  • K153128 — Kolplast Cervical Sample Collection Kit (January 13, 2017)
  • K141057 — DISPOSABLE CERVICAL BRUSH (May 14, 2015)
  • K111681 — HISTOBRUSH (January 19, 2012)
  • K083012 — PAPCONE (April 9, 2009)
  • K081522 — BIO NUCLEAR DIAGNOSTICS (ENDO)CERVICAL SAMPLER FOR GYN CYTOLOGY (December 5, 2008)
  • K072381 — SOFTPAP CERVICAL CELL COLLECTOR (January 30, 2008)
  • K062433 — DIAMICS CERCOL CERVICAL SAMPLE COLLECTOR SYSTEM (March 16, 2007)
  • K043369 — CERVEX-BRUSH COMBI (February 2, 2005)
  • K042527 — SPATULA, CERVICAL, CYTOLOGICAL, MODEL 22-9107 (November 8, 2004)

FDA data resources