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FDA 510(k)

LEGACY® IPC

K-Number: K232006 · 2023-08-04

ApplicantIg Technology, Ltd.
Decision Date2023-08-04
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LEGACY® IPC is the device name listed in this FDA 510(k) record. The listed applicant is Ig Technology, Ltd.. It received FDA 510(k) clearance on 2023-08-04 under 510(k) number K232006. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LEGACY® IPC?

LEGACY® IPC is a medical device that received FDA 510(k) clearance on 2023-08-04. The listed applicant is Ig Technology, Ltd.. The 510(k) number is K232006.

When did LEGACY® IPC receive FDA 510(k) clearance?

LEGACY® IPC received FDA 510(k) clearance on 2023-08-04, under 510(k) number K232006.

Who is the listed applicant for LEGACY® IPC?

The FDA 510(k) record lists Ig Technology, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LEGACY® IPC?

The FDA product code for LEGACY® IPC is JOW.

Related Devices (Code: JOW)

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.

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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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