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FDA 510(k)

TUTU 7, MODEL IV-T22

K-Number: K062735 · 2006-10-27

ApplicantInvisible Technology Co., Ltd.
Decision Date2006-10-27
Product CodeEBZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TUTU 7, MODEL IV-T22 is the device name listed in this FDA 510(k) record. The listed applicant is Invisible Technology Co., Ltd.. It received FDA 510(k) clearance on 2006-10-27 under 510(k) number K062735. The device is classified under product code EBZ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TUTU 7, MODEL IV-T22?

TUTU 7, MODEL IV-T22 is a medical device that received FDA 510(k) clearance on 2006-10-27. The listed applicant is Invisible Technology Co., Ltd.. The 510(k) number is K062735.

When did TUTU 7, MODEL IV-T22 receive FDA 510(k) clearance?

TUTU 7, MODEL IV-T22 received FDA 510(k) clearance on 2006-10-27, under 510(k) number K062735.

Who is the listed applicant for TUTU 7, MODEL IV-T22?

The FDA 510(k) record lists Invisible Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TUTU 7, MODEL IV-T22?

The FDA product code for TUTU 7, MODEL IV-T22 is EBZ.

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Related Devices (Code: EBZ)

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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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