510(k) K230051
K230051 is an FDA 510(k) premarket notification submitted by Boston Scientific Corporation for the device "14F iSLEEVE Introducer Set". The FDA issued a decision of Substantially Equivalent on Feb 3, 2023. The device falls under product code DYB (Introducer, Catheter), a Class II device regulated under 21 CFR 870.1340. Boston Scientific Corporation has 238 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Feb 3, 2023
- Date Received
- Jan 6, 2023
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Introducer, Catheter
- Device Class
- Class II
- Regulation Number
- 870.1340
- Review Panel
- CV
- Submission Type
- 510(k)