The following data is part of a premarket notification filed by Pjur Group Luxembourg Sa with the FDA for Pjur Aqua Baseline, Pjur Aqua Guarana, Pjur Aqua Provitamin B5, Pjur Back Door Anal Provitamin B5.
Device ID | K200731 |
510k Number | K200731 |
Device Name: | Pjur AQUA Baseline, Pjur AQUA Guarana, Pjur AQUA ProVitamin B5, Pjur BACK DOOR Anal Provitamin B5 |
Classification | Lubricant, Personal |
Applicant | pjur Group Luxembourg SA 87 Esplanade De La Moselle Wasserbillig, LU L-6637 |
Contact | Andrea Giebel |
Correspondent | Candace Cederman Candace F. Cederman 722 Arjean Drive Wilmington, NC 28411 |
Product Code | NUC |
CFR Regulation Number | 884.5300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2020-03-20 |
Decision Date | 2021-01-21 |