K-number	K122060
Device name	CLEVER TD-7001NEBULIZER
Applicant	Taidoc Technology Corporation
Product code	CAF
Device class	Class II
Decision date	Mar 21, 2013
Decision	Substantially Equivalent
Regulation	868.5630

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Source

View the full FDA submission: accessdata.fda.gov

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CLEVER TD-7001NEBULIZER

Everything you need for a 510(k) submission. Nothing you don't.