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FDA 510(k)

LC THERAPY, MODEL LCT-1000

K-Number: K070400 · 2007-02-28

ApplicantLitecure, LLC
Decision Date2007-02-28
Product CodeILY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

LC THERAPY, MODEL LCT-1000 is the device name listed in this FDA 510(k) record. The listed applicant is Litecure, LLC. It received FDA 510(k) clearance on 2007-02-28 under 510(k) number K070400. 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 LC THERAPY, MODEL LCT-1000?

LC THERAPY, MODEL LCT-1000 is a medical device that received FDA 510(k) clearance on 2007-02-28. The listed applicant is Litecure, LLC. The 510(k) number is K070400.

When did LC THERAPY, MODEL LCT-1000 receive FDA 510(k) clearance?

LC THERAPY, MODEL LCT-1000 received FDA 510(k) clearance on 2007-02-28, under 510(k) number K070400.

Who is the listed applicant for LC THERAPY, MODEL LCT-1000?

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

What is the FDA product code for LC THERAPY, MODEL LCT-1000?

The FDA product code for LC THERAPY, MODEL LCT-1000 is ILY.

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Other records listing Litecure, LLC as applicant

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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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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