P.A.S. Port Elite Implantable Venous Access System

• • Terminated Z-0067-2007 FDA Unclassified (pre-2012) ·initiated 27 Sep 2006 ·on shared 510(k) K992880

  Smiths Medical became aware that product returned to them under recall # Z-0800-06/ Z-0807-06 was inadvertently distributed to consignees after the recall was initiated 03/29/2006. The product was originally recalled because Locator Wand covers, which are supplied on the outside of PORT-A-CATH and P.A.S. PORT sterile trays, may have an insufficient seal and product sterility could be compromised.

• • Terminated Z-0806-06 FDA Unclassified (pre-2012) ·initiated 29 Mar 2006 ·on shared 510(k) K992880

  One lot of Locator-Wand Cover sterile pouches may have an insufficient seal and product sterility could be compromised. The Locator-Wand Cover is supplied with the PORT-A-CATH II AND P.A.S. PORT systems. The packaged Wand-Cover is placed on the outside of the PORT-A-CATH II AND P.A.S. PORT tray.

Recalls on a shared submission name another device cleared under the same FDA submission as this one.

510(k) Number

K992880 ↗

FDA Product Code

LJT

Device Class

Class II

Regulation

21 CFR Part 880.5965

Advisory Committee

General Hospital

FDA Decision

SESE Substantially Equivalent

• Port-A-Cath P.A.S. Port II Implantable Venous Access Sytems

  Class II

  FDA 510(k) K961580 Active Cleared 20 Sep 1996

• Sims Silo Needle De-Access Enclosure

  Class II

  FDA 510(k) K935767 Active Cleared 15 Nov 1995

• Port-A-Cath II Trans-Arterial Percutaneous System

  Class II

  FDA 510(k) K992697 Active Cleared 18 Nov 1999

• Cadd Administration Set, Cadd 250ml Flexible Medication Reservoir, Modified Securit Shell, Security Shell Adapter

  Class II

  FDA 510(k) K990083 Active Cleared 12 Feb 1999

• Port-A-Cath Low-Profile Implantable Access Systems

  Class II

  FDA 510(k) K973862 Active Cleared 29 Dec 1997

• Cadd Administration Set

  Class II

  FDA 510(k) K991599 Active Cleared 15 Jun 1999

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