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FDA 510(k)

AL T LASER, MODEL AVI HPLL-12

K-Number: K091285 · 2009-07-28

ApplicantAvicenna Laser Technology, Inc.
Decision Date2009-07-28
Product CodeILY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

AL T LASER, MODEL AVI HPLL-12 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 2009-07-28 under 510(k) number K091285. 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 AL T LASER, MODEL AVI HPLL-12?

AL T LASER, MODEL AVI HPLL-12 is a medical device that received FDA 510(k) clearance on 2009-07-28. The listed applicant is Avicenna Laser Technology, Inc.. The 510(k) number is K091285.

When did AL T LASER, MODEL AVI HPLL-12 receive FDA 510(k) clearance?

AL T LASER, MODEL AVI HPLL-12 received FDA 510(k) clearance on 2009-07-28, under 510(k) number K091285.

Who is the listed applicant for AL T LASER, MODEL AVI HPLL-12?

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 AL T LASER, MODEL AVI HPLL-12?

The FDA product code for AL T LASER, MODEL AVI HPLL-12 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.

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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.

K031612ALT LASER, MODEL VTR 75

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.

K253965CureLight Medical Diode Laser Systems (CureLight F2-A15; CureLight F2-B15; CureLight F2-A30; CureLight F2-B30; CureLight F3-AB30; CureLight F3-AB60.)Wuhan PHOMED Technology Company , Ltd.K242755Medical Diode Laser Systems (VELAS II-30B, VELAS II-30A, GBOX-15AB, GBOX-20B, CHEESE II-10B)Gigaalaser Company , Ltd.K231997SIRONA 100 Therapy Laser System (OEM's Model EVANLAS)Cure Point Therapeutics, Inc.K223642LED Lip Perfector, model: ZC-05Light Tree Ventures Europe B.V.K221189OLIZ LTB-1000ALtbio Co., Ltd.K213524CytonPro-5000Cytonsys, Inc.

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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