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FDA 510(k)

SCIg60 Infusion System

K-Number: K222087 · 2022-10-13

Decision Date2022-10-13
Product CodePKP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SCIg60 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 2022-10-13 under 510(k) number K222087. 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 SCIg60 Infusion System?

SCIg60 Infusion System is a medical device that received FDA 510(k) clearance on 2022-10-13. The listed applicant is Emed Technologies Corporation. The 510(k) number is K222087.

When did SCIg60 Infusion System receive FDA 510(k) clearance?

SCIg60 Infusion System received FDA 510(k) clearance on 2022-10-13, under 510(k) number K222087.

Who is the listed applicant for SCIg60 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 SCIg60 Infusion System?

The FDA product code for SCIg60 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.

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.

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.