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FDA 510(k)

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 the device name listed in this FDA 510(k) record. The listed applicant is Pjur Group Luxembourg S.A.. It received FDA 510(k) clearance on 2020-12-17 under 510(k) 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. The listed applicant is Pjur Group Luxembourg S.A.. The 510(k) number is K200730.

When did pjur WOMAN Nude pjur med SENSITIVE glide receive FDA 510(k) clearance?

pjur WOMAN Nude pjur med SENSITIVE glide received FDA 510(k) clearance on 2020-12-17, under 510(k) number K200730.

Who is the listed applicant for pjur WOMAN Nude pjur med SENSITIVE glide?

The FDA 510(k) record lists Pjur Group Luxembourg S.A. as the applicant. This does not by itself establish the device manufacturer.

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.

Other records listing Pjur Group Luxembourg S.A. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K260068pjur NATURE Touch, 100 mlK200527pjur WOMAN Aloe, pjur analyse me! water-based, pjur BACK DOOR water-based, pjur med Moisturising glide,pjur med NATURAL glide, We-Vibe Lube made by pjurK200731pjur AQUA Baseline, pjur AQUA Guarana, pjur AQUA ProVitamin B5, pjur BACK DOOR anal Provitamin B5

Related Devices (Code: NUC)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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.

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