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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 the device name listed in this FDA 510(k) record. The listed applicant is Emed Technologies Corporation. It received FDA 510(k) clearance on 2023-11-28 under 510(k) 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. The listed applicant is Emed Technologies Corporation. The 510(k) number is K230883.

When did VersaPump Infusion System receive FDA 510(k) clearance?

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

Who is the listed applicant for VersaPump Infusion System?

The FDA 510(k) record lists Emed Technologies Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VersaPump Infusion System?

The FDA product code for VersaPump Infusion System is PKP.

Other records listing Emed Technologies Corporation as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K251105Tetra (TM-20); Tetra (TM-50)K240148SCIg60 Infusion SystemK213429AccuSert Needle InserterK222087SCIg60 Infusion SystemK173783SCIg60 Infusion SystemK161906SCIg60 Infuser

View all 7 devices →

Related Devices (Code: PKP)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K251105Tetra (TM-20); Tetra (TM-50)Emed Technologies CorporationK240148SCIg60 Infusion SystemEmed Technologies CorporationK222087SCIg60 Infusion SystemEmed Technologies CorporationK173783SCIg60 Infusion SystemEmed Technologies CorporationK161906SCIg60 InfuserEmed 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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