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FDA 510(k)

MED-LOGICS, MODEL ML7090

K-Number: K033293 · 2004-01-13

Decision Date2004-01-13
Product CodeHNO
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MED-LOGICS, MODEL ML7090 is the device name listed in this FDA 510(k) record. The listed applicant is Med-Logics, Inc.. It received FDA 510(k) clearance on 2004-01-13 under 510(k) number K033293. The device is classified under product code HNO. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MED-LOGICS, MODEL ML7090?

MED-LOGICS, MODEL ML7090 is a medical device that received FDA 510(k) clearance on 2004-01-13. The listed applicant is Med-Logics, Inc.. The 510(k) number is K033293.

When did MED-LOGICS, MODEL ML7090 receive FDA 510(k) clearance?

MED-LOGICS, MODEL ML7090 received FDA 510(k) clearance on 2004-01-13, under 510(k) number K033293.

Who is the listed applicant for MED-LOGICS, MODEL ML7090?

The FDA 510(k) record lists Med-Logics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MED-LOGICS, MODEL ML7090?

The FDA product code for MED-LOGICS, MODEL ML7090 is HNO.

Related Clinical Trials

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.

Other records listing Med-Logics, Inc. 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 12 devices →

Related Devices (Code: HNO)

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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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