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FDA 510(k)

TQ SOLO AND SOLO PRO AND LS50 ACCESSORY AND MR4 MULTI RADIANCE THERAPY SYSTEM

K-Number: K080102 · 2008-08-20

ApplicantEscada International, Inc.
Decision Date2008-08-20
Product CodeILY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TQ SOLO AND SOLO PRO AND LS50 ACCESSORY AND MR4 MULTI RADIANCE THERAPY SYSTEM 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 2008-08-20 under 510(k) number K080102. 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 TQ SOLO AND SOLO PRO AND LS50 ACCESSORY AND MR4 MULTI RADIANCE THERAPY SYSTEM?

TQ SOLO AND SOLO PRO AND LS50 ACCESSORY AND MR4 MULTI RADIANCE THERAPY SYSTEM is a medical device that received FDA 510(k) clearance on 2008-08-20. The listed applicant is Escada International, Inc.. The 510(k) number is K080102.

When did TQ SOLO AND SOLO PRO AND LS50 ACCESSORY AND MR4 MULTI RADIANCE THERAPY SYSTEM receive FDA 510(k) clearance?

TQ SOLO AND SOLO PRO AND LS50 ACCESSORY AND MR4 MULTI RADIANCE THERAPY SYSTEM received FDA 510(k) clearance on 2008-08-20, under 510(k) number K080102.

Who is the listed applicant for TQ SOLO AND SOLO PRO AND LS50 ACCESSORY AND MR4 MULTI RADIANCE THERAPY SYSTEM?

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 TQ SOLO AND SOLO PRO AND LS50 ACCESSORY AND MR4 MULTI RADIANCE THERAPY SYSTEM?

The FDA product code for TQ SOLO AND SOLO PRO AND LS50 ACCESSORY AND MR4 MULTI RADIANCE THERAPY SYSTEM is ILY.

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Other records listing Escada International, Inc. as applicant

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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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