510(k) K220489

Durex Patronus CloseFit, Durex Patronus Regular by Rb Health (Us), LLC — Product Code HIS

K220489 is an FDA 510(k) premarket notification submitted by Rb Health (Us), LLC for the device "Durex Patronus CloseFit, Durex Patronus Regular". The FDA issued a decision of Substantially Equivalent on November 7, 2022. The device falls under product code HIS (Condom), a Class II device regulated under 21 CFR 884.5300. Rb Health (Us), LLC has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 7, 2022
Date Received
February 22, 2022
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Condom
Device Class
Class II
Regulation Number
884.5300
Review Panel
OB
Submission Type