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FDA 510(k)

TERRAQUANT MQ2000 V.5 WITH THE TQ-1TENS

K-Number: K071445 · 2007-10-29

ApplicantEscada International, Inc.
Decision Date2007-10-29
Product CodeILY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TERRAQUANT MQ2000 V.5 WITH THE TQ-1TENS 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 2007-10-29 under 510(k) number K071445. 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 WITH THE TQ-1TENS?

TERRAQUANT MQ2000 V.5 WITH THE TQ-1TENS is a medical device that received FDA 510(k) clearance on 2007-10-29. The listed applicant is Escada International, Inc.. The 510(k) number is K071445.

When did TERRAQUANT MQ2000 V.5 WITH THE TQ-1TENS receive FDA 510(k) clearance?

TERRAQUANT MQ2000 V.5 WITH THE TQ-1TENS received FDA 510(k) clearance on 2007-10-29, under 510(k) number K071445.

Who is the listed applicant for TERRAQUANT MQ2000 V.5 WITH THE TQ-1TENS?

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 WITH THE TQ-1TENS?

The FDA product code for TERRAQUANT MQ2000 V.5 WITH THE TQ-1TENS 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 SYSTEMK061614TERRAQUANT MQ2000 V. 5 AND HANDYRX MQ2007 LASERSK043055TERRAQUANT 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.

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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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