510(k) K142817
K142817 is an FDA 510(k) premarket notification submitted by Texasmedical Technologies, Inc. for the device "IntraNovo 25 Microcatheter". The FDA issued a decision of Substantially Equivalent on Apr 23, 2015. The device falls under product code DQO (Catheter, Intravascular, Diagnostic), a Class II device regulated under 21 CFR 870.1200. Texasmedical Technologies, Inc. has 6 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Apr 23, 2015
- Date Received
- Sep 29, 2014
- 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)