K-number	K200629
Device name	Aspire Mechanical Aspirator G
Applicant	Control Medical Technology
Product code	FMF
Device class	Class II
Decision date	May 29, 2020
Decision	Substantially Equivalent
Regulation	880.5860

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Source

View the full FDA submission: accessdata.fda.gov

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Aspire Mechanical Aspirator G

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