FDA 510(k) FDA class 2 Substantially Equivalent 🇱🇺 Luxembourg

pjur AQUA Baseline, pjur AQUA Guarana, pjur AQUA ProVitamin B5, pjur BACK DOOR anal Provitamin B5

K Number: K200731 · Decision Jan 21, 2021
Classifications
1
FEI Numbers
123
Registration Numbers
123
Same Product Code
242
Applicant Total
7
Review Days
307

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Basic Information

Device Name
pjur AQUA Baseline, pjur AQUA Guarana, pjur AQUA ProVitamin B5, pjur BACK DOOR anal Provitamin B5
K Number
K200731
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.5300
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Pjur Group Luxembourg S.A.
Date Received
March 20, 2020
Decision Date
January 21, 2021
Product Code
NUC
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
NUC Lubricant, Personal

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Other Clearances by Pjur Group Luxembourg S.A.

K Number Device Name
K260068 pjur NATURE Touch, 100 ml
K200527 pjur 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 pjur
K200730 pjur WOMAN Nude pjur med SENSITIVE glide
K141913 PJUR SILICONE BASED LUBRICANT: PJUR BACKDOOR ANAL GLIDE AND ANALYSE ME!
K133336 PJUR(R) SILICONEGEL, PJUR(R) BASIC PERSONAL GLIDE, PJUR(R) LIGHT, PJUR(R) MED PREMIUM GLIDE
K133233 PJUR ORIGINAL, PJUR WOMAN, PJUR MAN EXTREME GLIDE