K-number	K170591
Device name	Altomed Malhotra Platinum Segments
Applicant	Altomed Limited
Product code	MML
Device class	Class II
Decision date	Jun 6, 2017
Decision	Substantially Equivalent
Regulation	886.5700

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Source

View the full FDA submission: accessdata.fda.gov

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Altomed Malhotra Platinum Segments

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