pjur WOMAN Nude pjur med SENSITIVE glide (K200730) — FDA 510(k) Clearance | Predicase

K-number	K200730
Device name	pjur WOMAN Nude pjur med SENSITIVE glide
Applicant	Pjur Group Luxembourg S.A.
Product code	NUC
Device class	Class II
Decision date	Dec 17, 2020
Decision	Substantially Equivalent
Regulation	884.5300

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View the full FDA submission: accessdata.fda.gov

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