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FDA 510(k)

DPL THERAPY SYSTEM

K-Number: K081570 · 2008-11-07

ApplicantLed Technologies, LLC
Decision Date2008-11-07
Product CodeILY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

DPL THERAPY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Led Technologies, LLC. It received FDA 510(k) clearance on 2008-11-07 under 510(k) number K081570. 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 DPL THERAPY SYSTEM?

DPL THERAPY SYSTEM is a medical device that received FDA 510(k) clearance on 2008-11-07. The listed applicant is Led Technologies, LLC. The 510(k) number is K081570.

When did DPL THERAPY SYSTEM receive FDA 510(k) clearance?

DPL THERAPY SYSTEM received FDA 510(k) clearance on 2008-11-07, under 510(k) number K081570.

Who is the listed applicant for DPL THERAPY SYSTEM?

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

What is the FDA product code for DPL THERAPY SYSTEM?

The FDA product code for DPL THERAPY SYSTEM 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 Led Technologies, LLC 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.

K101382DPL NUVE

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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