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FDA 510(k)

MI-15 EXAM SURGICAL LIGHT

K-Number: K930897 · 1993-06-25

Decision Date1993-06-25
Product CodeFTD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MI-15 EXAM SURGICAL LIGHT is the device name listed in this FDA 510(k) record. The listed applicant is Medical Illumination, Inc.. It received FDA 510(k) clearance on 1993-06-25 under 510(k) number K930897. The device is classified under product code FTD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MI-15 EXAM SURGICAL LIGHT?

MI-15 EXAM SURGICAL LIGHT is a medical device that received FDA 510(k) clearance on 1993-06-25. The listed applicant is Medical Illumination, Inc.. The 510(k) number is K930897.

When did MI-15 EXAM SURGICAL LIGHT receive FDA 510(k) clearance?

MI-15 EXAM SURGICAL LIGHT received FDA 510(k) clearance on 1993-06-25, under 510(k) number K930897.

Who is the listed applicant for MI-15 EXAM SURGICAL LIGHT?

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

What is the FDA product code for MI-15 EXAM SURGICAL LIGHT?

The FDA product code for MI-15 EXAM SURGICAL LIGHT is FTD.

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 Medical Illumination, 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.

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Related Devices (Code: FTD)

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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