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510(k) K230883

VersaPump Infusion System by Emed Technologies Corporation — Product Code PKP

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 28, 2023
Date Received
March 30, 2023
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Immunoglobulin G (Igg) Infusion System
Device Class
Class II
Regulation Number
880.5725
Review Panel
HO
Submission Type

An Immunoglobulin G (IgG) Infusion System is a prescription device intended for subcutaneous delivery of Immunoglobulin G (IgG) in accordance with the FDA approved labeling.

Other clearances by Emed Technologies Corporation

  • K251105 — Tetra (TM-20); Tetra (TM-50) (December 22, 2025)
  • K240148 — SCIg60 Infusion System (February 16, 2024)
  • K213429 — AccuSert Needle Inserter (October 20, 2022)
  • K222087 — SCIg60 Infusion System (October 13, 2022)
  • K173783 — SCIg60 Infusion System (December 14, 2018)
  • K161906 — SCIg60 Infuser (December 1, 2016)
  • K142319 — SCIg60 Infuser, Infuset (May 14, 2015)
  • K140133 — INFUSET FLOW CONTROL EXTENSION SET (May 15, 2014)
  • K140131 — SUB-Q SUBCUTANEOUS TISSUE INFUSION SET (April 3, 2014)
  • K123729 — VERSARATE FLOW RATE CONTROLER (December 21, 2012)

Other clearances for product code PKP

  • K251105 — Tetra (TM-20); Tetra (TM-50) (December 22, 2025)
  • K240148 — SCIg60 Infusion System (February 16, 2024)
  • K222087 — SCIg60 Infusion System (October 13, 2022)
  • K173783 — SCIg60 Infusion System (December 14, 2018)
  • K161906 — SCIg60 Infuser (December 1, 2016)
  • K142319 — SCIg60 Infuser, Infuset (May 14, 2015)