510(k) K233824
K233824 is an FDA 510(k) premarket notification submitted by Edwards Lifesciences, LLC for the device "Swan-Ganz catheter". The FDA issued a decision of Substantially Equivalent on June 6, 2024. The device falls under product code DYG (Catheter, Flow Directed), a Class II device regulated under 21 CFR 870.1240. Edwards Lifesciences, LLC has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 6, 2024
- Date Received
- December 1, 2023
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Catheter, Flow Directed
- Device Class
- Class II
- Regulation Number
- 870.1240
- Review Panel
- CV
- Submission Type