Contour-Port

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K912540 ↗

FDA Product Code

LJT

Device Class

Class II

Regulation

21 CFR Part 880.5965

Advisory Committee

General Hospital

FDA Decision

SESK Substantially Equivalent — Kit

• Tri-Lumen Intra Vascular Balloon Catheter (Gu Use)

  Class II

  FDA 510(k) K891588 Active Cleared 28 Sep 1989

• Tri-Lumen Intra Vascular Balloon Catheter

  Class II

  FDA 510(k) K891021 Active Cleared 18 Sep 1989

• Ideas' Port

  Class II

  FDA 510(k) K913602 Active Cleared 2 Jan 1992

• Grice Soft Tissue Biopsy Kit

  Class II

  FDA 510(k) K922161 Active Cleared 13 Oct 1992

• Ideas Peanut Wand

  Class II

  FDA 510(k) K926335 Active Cleared 24 Jun 1993

• Grice Laparoscopic Suturing Needle

  Class II

  FDA 510(k) K921922 Active Cleared 8 Jul 1992

See all devices from Ideal Medical, Inc. →