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FDA 510(k)

TERRAQUANT MQ2000 V. 5 AND HANDYRX MQ2007 LASERS

K-Number: K061614 · 2006-10-06

ApplicantEscada International, Inc.
Decision Date2006-10-06
Product CodeILY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TERRAQUANT MQ2000 V. 5 AND HANDYRX MQ2007 LASERS is the device name listed in this FDA 510(k) record. The listed applicant is Escada International, Inc.. It received FDA 510(k) clearance on 2006-10-06 under 510(k) number K061614. 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 TERRAQUANT MQ2000 V. 5 AND HANDYRX MQ2007 LASERS?

TERRAQUANT MQ2000 V. 5 AND HANDYRX MQ2007 LASERS is a medical device that received FDA 510(k) clearance on 2006-10-06. The listed applicant is Escada International, Inc.. The 510(k) number is K061614.

When did TERRAQUANT MQ2000 V. 5 AND HANDYRX MQ2007 LASERS receive FDA 510(k) clearance?

TERRAQUANT MQ2000 V. 5 AND HANDYRX MQ2007 LASERS received FDA 510(k) clearance on 2006-10-06, under 510(k) number K061614.

Who is the listed applicant for TERRAQUANT MQ2000 V. 5 AND HANDYRX MQ2007 LASERS?

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

What is the FDA product code for TERRAQUANT MQ2000 V. 5 AND HANDYRX MQ2007 LASERS?

The FDA product code for TERRAQUANT MQ2000 V. 5 AND HANDYRX MQ2007 LASERS is ILY.

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Other records listing Escada International, 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.

K080102TQ SOLO AND SOLO PRO AND LS50 ACCESSORY AND MR4 MULTI RADIANCE THERAPY SYSTEMK071445TERRAQUANT MQ2000 V.5 WITH THE TQ-1TENSK043055TERRAQUANT MQ2000 LASER THERAPY DEVICE

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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