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FDA 510(k)

ML830TP

K-Number: K080786 · 2008-10-03

ApplicantMicrolight Corporation of America
Decision Date2008-10-03
Product CodeILY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ML830TP is the device name listed in this FDA 510(k) record. The listed applicant is Microlight Corporation of America. It received FDA 510(k) clearance on 2008-10-03 under 510(k) number K080786. The device is classified under product code ILY. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ML830TP?

ML830TP is a medical device that received FDA 510(k) clearance on 2008-10-03. The listed applicant is Microlight Corporation of America. The 510(k) number is K080786.

When did ML830TP receive FDA 510(k) clearance?

ML830TP received FDA 510(k) clearance on 2008-10-03, under 510(k) number K080786.

Who is the listed applicant for ML830TP?

The FDA 510(k) record lists Microlight Corporation of America as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ML830TP?

The FDA product code for ML830TP is ILY.

Other records listing Microlight Corporation of America 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.

K041364ML830 LASER SYSTEMK010175MICROLIGHT 830 LASER SYSTEM

Related Devices (Code: ILY)

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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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