510(k) K210509
K210509 is an FDA 510(k) premarket notification submitted by Rocket Medical Plc for the device "Rocket Platinum Cured Cathter". The FDA issued a decision of Substantially Equivalent (kit) on September 9, 2021. The device falls under product code DWM (Apparatus, Suction, Patient Care), a Class II device regulated under 21 CFR 870.5050. Rocket Medical Plc has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESK (Substantially Equivalent (kit))
- Decision Date
- September 9, 2021
- Date Received
- February 22, 2021
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Apparatus, Suction, Patient Care
- Device Class
- Class II
- Regulation Number
- 870.5050
- Review Panel
- AN
- Submission Type