510(k) K050472
K050472 is an FDA 510(k) premarket notification submitted by Ekos Corp. for the device "LYSUS INFUSION SYSTEM". The FDA issued a decision of Substantially Equivalent on March 11, 2005. The device falls under product code DRA (Catheter, Steerable), a Class II device regulated under 21 CFR 870.1280. Ekos Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 11, 2005
- Date Received
- February 24, 2005
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Catheter, Steerable
- Device Class
- Class II
- Regulation Number
- 870.1280
- Review Panel
- CV
- Submission Type