pjur WOMAN Nude pjur med SENSITIVE glide
K-Number: K200730 · 2020-12-17
ApplicantPjur Group Luxembourg S.A.
Decision Date2020-12-17
Product CodeNUC
Advisory CommitteeOB
DecisionSubstantially Equivalent
Device Summary
pjur WOMAN Nude pjur med SENSITIVE glide is a medical device manufactured by Pjur Group Luxembourg S.A.. It received FDA 510(k) clearance on 2020-12-17 under approval number K200730. The device is classified under product code NUC. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the pjur WOMAN Nude pjur med SENSITIVE glide?
pjur WOMAN Nude pjur med SENSITIVE glide is a medical device that received FDA 510(k) clearance on 2020-12-17. It is manufactured by Pjur Group Luxembourg S.A.. The 510(k) number is K200730.
When was pjur WOMAN Nude pjur med SENSITIVE glide approved by the FDA?
pjur WOMAN Nude pjur med SENSITIVE glide received FDA 510(k) clearance on 2020-12-17, under approval number K200730.
What company makes pjur WOMAN Nude pjur med SENSITIVE glide?
pjur WOMAN Nude pjur med SENSITIVE glide is manufactured by Pjur Group Luxembourg S.A..
What is the FDA product code for pjur WOMAN Nude pjur med SENSITIVE glide?
The FDA product code for pjur WOMAN Nude pjur med SENSITIVE glide is NUC.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.