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510(k) K882190

S.E.A.-PORT(TM) VASCULAR ACCESS SYSTEM by Harbor Medical Devices, Inc. — Product Code LJT

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 9, 1988
Date Received
May 24, 1988
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Port & Catheter, Implanted, Subcutaneous, Intravascular
Device Class
Class II
Regulation Number
880.5965
Review Panel
HO
Submission Type

Other clearances by Harbor Medical Devices, Inc.

  • K884628 — HARBORIN CENTRAL VENOUS CATHETER (May 15, 1989)
  • K890518 — SINGLE LUMEN S.E.A.-PORT VASCULAR ACCESS SYSTEM (April 21, 1989)
  • K882657 — HARBOR S.E.A.-PORT SURGICAL ACCESSORY KIT (December 13, 1988)
  • K881884 — HARBOR CENTRAL VENOUS CATHETER (July 28, 1988)
  • K880297 — SEA - PORT INFUSION SET (February 19, 1988)
  • K874414 — HYPODERMIC NEEDLES, SINGLE LUMEN (January 14, 1988)

Other clearances for product code LJT

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  • K242328 — PowerPort™ ClearVUE™ Slim Implantable Ports and PowerPort™ ClearVUE™ Slim Implan (October 31, 2024)
  • K232737 — PowerPort™ ClearVUE™ Slim ECG Enabled Implantable Port; PowerPort™ ClearVUE™ isp (December 8, 2023)
  • K190559 — SmartPort+ Implantable Ports, SmartPort Plastic Implantable Ports (May 22, 2020)
  • K181446 — Bard Power-Injectable Implantable Ports (PowerPorts®) (July 8, 2019)
  • K151239 — NMI DUAL PORT II (June 6, 2016)
  • K153359 — BardPort®, SlimPort®, and X-Port® Implanted Ports (May 20, 2016)
  • K153238 — Dignity Dual Port (March 15, 2016)
  • K153228 — NMI Port, NMI Port II (December 4, 2015)