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FDA 510(k)

ISM1+, IMS2+, AND UTM+

K-Number: K030490 · 2003-08-20

ApplicantMedicult A/S
Decision Date2003-08-20
Product CodeMQL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

ISM1+, IMS2+, AND UTM+ is the device name listed in this FDA 510(k) record. The listed applicant is Medicult A/S. It received FDA 510(k) clearance on 2003-08-20 under 510(k) number K030490. The device is classified under product code MQL. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ISM1+, IMS2+, AND UTM+?

ISM1+, IMS2+, AND UTM+ is a medical device that received FDA 510(k) clearance on 2003-08-20. The listed applicant is Medicult A/S. The 510(k) number is K030490.

When did ISM1+, IMS2+, AND UTM+ receive FDA 510(k) clearance?

ISM1+, IMS2+, AND UTM+ received FDA 510(k) clearance on 2003-08-20, under 510(k) number K030490.

Who is the listed applicant for ISM1+, IMS2+, AND UTM+?

The FDA 510(k) record lists Medicult A/S as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ISM1+, IMS2+, AND UTM+?

The FDA product code for ISM1+, IMS2+, AND UTM+ is MQL.

Other records listing Medicult A/S 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 26 devices →

Related Devices (Code: MQL)

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.

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