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FDA 510(k)

CLEVER TD-7001NEBULIZER

K-Number: K122060 · 2013-03-21

ApplicantTaidoc Technology Corporation
Decision Date2013-03-21
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CLEVER TD-7001NEBULIZER is the device name listed in this FDA 510(k) record. The listed applicant is Taidoc Technology Corporation. It received FDA 510(k) clearance on 2013-03-21 under 510(k) number K122060. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLEVER TD-7001NEBULIZER?

CLEVER TD-7001NEBULIZER is a medical device that received FDA 510(k) clearance on 2013-03-21. The listed applicant is Taidoc Technology Corporation. The 510(k) number is K122060.

When did CLEVER TD-7001NEBULIZER receive FDA 510(k) clearance?

CLEVER TD-7001NEBULIZER received FDA 510(k) clearance on 2013-03-21, under 510(k) number K122060.

Who is the listed applicant for CLEVER TD-7001NEBULIZER?

The FDA 510(k) record lists Taidoc Technology Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CLEVER TD-7001NEBULIZER?

The FDA product code for CLEVER TD-7001NEBULIZER is CAF.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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