510(k) K223178
K223178 is an FDA 510(k) premarket notification submitted by Medtronic for the device "SelectSite C304 Deflectable Catheter System, C315 Delivery System". The FDA issued a decision of Substantially Equivalent on Nov 8, 2022. The device falls under product code DQY (Catheter, Percutaneous), a Class II device regulated under 21 CFR 870.1250. Medtronic has 247 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Nov 8, 2022
- Date Received
- Oct 11, 2022
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Catheter, Percutaneous
- Device Class
- Class II
- Regulation Number
- 870.1250
- Review Panel
- CV
- Submission Type
- 510(k)