Pharma-Plast Oxygen Catheter

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K843466 ↗

FDA Product Code

BZB

FDA applicant

Zimmar Consulting , Ltd.

Device Class

Class I

Regulation

21 CFR Part 868.5350

Advisory Committee

Anesthesiology

FDA Decision

SESE Substantially Equivalent

• Pharma-Plast Single Use Overshoes

  Class I

  FDA 510(k) K843475 Active Cleared 31 Oct 1984

• Pharma-Plast Insulin Syringe

  Class II

  FDA 510(k) K843473 Active Cleared 31 Oct 1984

• Pharma-Plast Connecting Tube Type Urin-

  Class II

  FDA 510(k) K843481 Active Cleared 18 Oct 1984

• Pharma-Plast Petri Dish

  Class I

  FDA 510(k) K843483 Active Cleared 21 Sep 1984

• Pharma-Plast Leg Bag

  Class II

  FDA 510(k) K843479 Active Cleared 11 Oct 1984

• Pharma-Plast Syringe With Needle

  Class II

  FDA 510(k) K843472 Active Cleared 31 Oct 1984

See all devices from Zimmar Consulting, Ltd. →