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FDA 510(k)

ALT LASER, MODEL VTR 75

K-Number: K031612 · 2003-12-11

Decision Date2003-12-11
Product CodeILY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ALT LASER, MODEL VTR 75 is the device name listed in this FDA 510(k) record. The listed applicant is Avicenna Laser Technology, Inc.. It received FDA 510(k) clearance on 2003-12-11 under 510(k) number K031612. 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 ALT LASER, MODEL VTR 75?

ALT LASER, MODEL VTR 75 is a medical device that received FDA 510(k) clearance on 2003-12-11. The listed applicant is Avicenna Laser Technology, Inc.. The 510(k) number is K031612.

When did ALT LASER, MODEL VTR 75 receive FDA 510(k) clearance?

ALT LASER, MODEL VTR 75 received FDA 510(k) clearance on 2003-12-11, under 510(k) number K031612.

Who is the listed applicant for ALT LASER, MODEL VTR 75?

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

What is the FDA product code for ALT LASER, MODEL VTR 75?

The FDA product code for ALT LASER, MODEL VTR 75 is ILY.

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 Avicenna Laser Technology, 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.

Related Devices (Code: ILY)

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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