K-number	K182292
Device name	VORTRAN APM-Plus
Applicant	Vortran Medical Technology 1, Inc.
Product code	CAP
Device class	Class II
Decision date	Sep 18, 2019
Decision	Substantially Equivalent
Regulation	868.2600

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Source

View the full FDA submission: accessdata.fda.gov

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VORTRAN APM-Plus

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