510(k) K210509

Rocket Platinum Cured Cathter by Rocket Medical Plc — Product Code DWM

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