510(k) K100840
K100840 is an FDA 510(k) premarket notification submitted by Hotspur Technologies for the device "EMBO PLUS EMBOLECTOMY CATHETER". The FDA issued a decision of Substantially Equivalent on July 12, 2010. The device falls under product code DXE (Catheter, Embolectomy), a Class II device regulated under 21 CFR 870.5150. Hotspur Technologies has at least 4 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 12, 2010
- Date Received
- March 24, 2010
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Catheter, Embolectomy
- Device Class
- Class II
- Regulation Number
- 870.5150
- Review Panel
- CV
- Submission Type