Mic-Key Sf Low Profile Gastrostomy Tube and Accessories

• • Terminated Z-2969-2020 FDA Class II ·initiated 29 Jul 2020

  Devices had cracked or detached from the feeding tube body

510(k) Number

K122653 ↗

FDA Product Code

KNT

FDA applicant

Kimberly-Clark Corporation

Device Class

Class II

Regulation

21 CFR Part 876.5980

Advisory Committee

Gastroenterology, Urology

FDA Decision

SESK Substantially Equivalent — Kit

• Kimberly-Clark Child's Facemask

  Class II

  FDA 510(k) K113340 Active Cleared 4 May 2012

• Kotex Profile Shaped Maxi Pad

  Class I

  FDA 510(k) K871210 Active Cleared 10 Apr 1987

• Kimberly-Clark Self-Seal Pouch for Low Temperature Sterilization

  Class II

  FDA 510(k) K973827 Active Cleared 11 Feb 1998

• Kotex Security Tube Tampons

  Class II

  FDA 510(k) K885194 Active Cleared 1 Mar 1989

• Spunguard Face Mask Open recall

  Class II

  FDA 510(k) K823078 Active Cleared 7 Jan 1983

• Kotex Super Maxi Pads

  Class II

  FDA 510(k) K890013 Active Cleared 25 Apr 1989

See all devices from Kimberly-Clark Corporation →