Byrd Telescoping Stainless Steel Dilat Sheath Set

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

510(k) Number

K922354 ↗

FDA Product Code

GCC

Device Class

Class I

Regulation

21 CFR Part 878.4200

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

• Vital-Port Infusion Pal

  Class II

  FDA 510(k) K971140 Active Cleared 17 Nov 1997

• Vital-Port Vascular Access System

  Class II

  FDA 510(k) K911449 Active Cleared 24 Jun 1991

• Vital-Port M.R.I. Vascular Access System 7012, 7112

  Class II

  FDA 510(k) K912423 Active Cleared 30 Jul 1991

• Vital-Port Mini Vascular Access System

  Class II

  FDA 510(k) K931586 Active Cleared 27 Sep 1993

• Wilson-Cook Colonic Z-Stent

  Class II

  FDA 510(k) K990034 Active Cleared 17 Apr 2000

• Vital-Port Dual Lumen Vascular Access System 1121

  Class II

  FDA 510(k) K912465 Active Cleared 30 Jul 1991

See all devices from Med Institute, Inc. →