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FDA 510(k)

VersaPump Infusion System

K-Number: K230883 · 2023-11-28

ApplicantEmed Technologies Corporation
Decision Date2023-11-28
Product CodePKP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VersaPump Infusion System is a medical device manufactured by Emed Technologies Corporation. It received FDA 510(k) clearance on 2023-11-28 under approval number K230883. The device is classified under product code PKP. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VersaPump Infusion System?

VersaPump Infusion System is a medical device that received FDA 510(k) clearance on 2023-11-28. It is manufactured by Emed Technologies Corporation. The 510(k) number is K230883.

When was VersaPump Infusion System approved by the FDA?

VersaPump Infusion System received FDA 510(k) clearance on 2023-11-28, under approval number K230883.

What company makes VersaPump Infusion System?

VersaPump Infusion System is manufactured by Emed Technologies Corporation.

What is the FDA product code for VersaPump Infusion System?

The FDA product code for VersaPump Infusion System is PKP.

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Other Devices by Emed Technologies Corporation

K161906SCIg60 Infuser K173783SCIg60 Infusion System K213429AccuSert Needle Inserter K222087SCIg60 Infusion System K240148SCIg60 Infusion System K251105Tetra (TM-20); Tetra (TM-50)

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Related Devices (Code: PKP)

K161906SCIg60 InfuserEmed Technologies Corporation K173783SCIg60 Infusion SystemEmed Technologies Corporation K222087SCIg60 Infusion SystemEmed Technologies Corporation K240148SCIg60 Infusion SystemEmed Technologies Corporation K251105Tetra (TM-20); Tetra (TM-50)Emed Technologies Corporation

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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