Sealer Solvent

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K241354 ↗

FDA Product Code

KJJ

Device Class

U

Advisory Committee

Unknown

FDA Decision

SESE Substantially Equivalent

• Foley Catheters

  Class II

  FDA 510(k) K781457 Active Cleared 20 Sep 1978

• Irrigation Tray

  Class II

  FDA 510(k) K781748 Active Cleared 12 Dec 1978

• Non Sterile Parenteral Supply Kit

  Class II

  FDA 510(k) K900857 Active Cleared 22 May 1990

• ReminGel

  Class II

  FDA 510(k) K241489 Active Cleared 8 Jan 2025

• Gen. Purpose Instrument Trays &

  Class I

  FDA 510(k) K833058 Active Cleared 31 Jan 1984

• Ureteral Stone Dislodger

  Class II

  FDA 510(k) K851922 Active Cleared 2 Aug 1985

See all devices from Intermed, Inc. →