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FDA 510(k)

microINR System

K-Number: K243543 · 2025-02-27

Decision Date2025-02-27
Product CodeGJS
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

microINR System is the device name listed in this FDA 510(k) record. The listed applicant is Iline Microsystems, S.L.. It received FDA 510(k) clearance on 2025-02-27 under 510(k) number K243543. The device is classified under product code GJS. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the microINR System?

microINR System is a medical device that received FDA 510(k) clearance on 2025-02-27. The listed applicant is Iline Microsystems, S.L.. The 510(k) number is K243543.

When did microINR System receive FDA 510(k) clearance?

microINR System received FDA 510(k) clearance on 2025-02-27, under 510(k) number K243543.

Who is the listed applicant for microINR System?

The FDA 510(k) record lists Iline Microsystems, S.L. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for microINR System?

The FDA product code for microINR System is GJS.

Other records listing Iline Microsystems, S.L. 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.

Related Devices (Code: GJS)

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

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