Pall Dental Filtration System with Air Water Syringe Housing and Filter Membrane

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

510(k) Number

K983735 ↗

FDA Product Code

EIA

Device Class

Class I

Regulation

21 CFR Part 872.6640

Advisory Committee

Dental

FDA Decision

SESE Substantially Equivalent

• Modification to Laparoshield Conditioned Insufflation Set

  Class II

  FDA 510(k) K033991 Active Cleared 22 Jan 2004

• Pall Surgiclear Laparoscopic Smoke Filtration System, Model CLSF1

  Class II

  FDA 510(k) K992361 Active Cleared 20 Aug 1999

• Pall Dental Filtration System with Inline Handpiece Housing and Filter Membrane

  Class I

  FDA 510(k) K983731 Active Cleared 21 Dec 1998

• Pall Ultipor Anesthesia Breathing System

  Class II

  FDA 510(k) K013093 Active Cleared 1 Aug 2002

• Laparoshield Conditioned Insufflation Set

  Class II

  FDA 510(k) K030469 Active Cleared 9 May 2003