K-number	K221604
Device name	SafetiHeel, MediHeel, Novaplus
Applicant	Nsp Tech Pte, Ltd.
Product code	FMK
Device class	Class II
Decision date	Aug 22, 2022
Decision	Substantially Equivalent
Regulation	878.4850

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Source

View the full FDA submission: accessdata.fda.gov

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SafetiHeel, MediHeel, Novaplus

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