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FDA 510(k)

MODEL LA-1200 MULTI-CHANNEL LASER THERAPY SYSTEM

K-Number: K102134 · 2010-12-23

ApplicantUnited Integrated Services Co., Ltd.
Decision Date2010-12-23
Product CodeILY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MODEL LA-1200 MULTI-CHANNEL LASER THERAPY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is United Integrated Services Co., Ltd.. It received FDA 510(k) clearance on 2010-12-23 under 510(k) number K102134. 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 MODEL LA-1200 MULTI-CHANNEL LASER THERAPY SYSTEM?

MODEL LA-1200 MULTI-CHANNEL LASER THERAPY SYSTEM is a medical device that received FDA 510(k) clearance on 2010-12-23. The listed applicant is United Integrated Services Co., Ltd.. The 510(k) number is K102134.

When did MODEL LA-1200 MULTI-CHANNEL LASER THERAPY SYSTEM receive FDA 510(k) clearance?

MODEL LA-1200 MULTI-CHANNEL LASER THERAPY SYSTEM received FDA 510(k) clearance on 2010-12-23, under 510(k) number K102134.

Who is the listed applicant for MODEL LA-1200 MULTI-CHANNEL LASER THERAPY SYSTEM?

The FDA 510(k) record lists United Integrated Services Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL LA-1200 MULTI-CHANNEL LASER THERAPY SYSTEM?

The FDA product code for MODEL LA-1200 MULTI-CHANNEL LASER THERAPY SYSTEM is ILY.

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Other records listing United Integrated Services Co., Ltd. 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.

K111771NON-CONTACT TEAR FILM THERMOGRAGHK082686MULTI-CHANNEL LASER THERAPY SYSTEM

Related Devices (Code: ILY)

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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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