510(k) K213647
K213647 is an FDA 510(k) premarket notification submitted by Rb Health (Us), LLC for the device "Durex Patronus Wide". The FDA issued a decision of Substantially Equivalent on February 17, 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
- February 17, 2022
- Date Received
- November 19, 2021
- 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