Vitalcare I.V. Administration Set

No FDA recalls on record, checked 26 Oct 2026.

510(k) Number

K050906 ↗

FDA Product Code

FPA

Device Class

Class II

Regulation

21 CFR Part 880.5440

Advisory Committee

General Hospital

FDA Decision

SESE Substantially Equivalent

• Vitalcare Disposable Vaginal Speculum

  Class II

  FDA 510(k) K983716 Active Cleared 23 Dec 1998

• Vitalcare Powder Free Synthetic Vinyl Examination Glove

  Class I

  FDA 510(k) K040916 Active Cleared 4 May 2005

• Vitalcare Sterilewater and 0.9% Sodium Chloride Pre-Filled 10cc/30cc Syringes

  Class II

  FDA 510(k) K031748 Active Cleared 27 Aug 2003

• Vinyl Powdered Exam Glove / Cat.# 15-020

  Class I

  FDA 510(k) K992289 Active Cleared 4 Aug 1999

• Latex Patient Examination Glove, Cat. No. 1000M Powdered

  Class I

  FDA 510(k) K982901 Active Cleared 21 Dec 1998

• Omi Retractable Safety Syringe

  Class II

  FDA 510(k) K060109 Active Cleared 5 May 2006

See all devices from Vitalcare Group, Inc. →