510(k) K150232
K150232 is an FDA 510(k) premarket notification submitted by Ashitaka Factory Of Terumo Corp. for the device "Radifocus Optitorque Angiographic Catheter". The FDA issued a decision of Substantially Equivalent on Oct 19, 2015. The device falls under product code DQO (Catheter, Intravascular, Diagnostic), a Class II device regulated under 21 CFR 870.1200. Ashitaka Factory Of Terumo Corp. has 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Oct 19, 2015
- Date Received
- Feb 2, 2015
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Catheter, Intravascular, Diagnostic
- Device Class
- Class II
- Regulation Number
- 870.1200
- Review Panel
- CV
- Submission Type
- 510(k)