510(k) K925813
K925813 is an FDA 510(k) premarket notification submitted by Target Therapeutics for the device "DIAGNOSTIC INTRAVASCULAR CATHETER". The FDA issued a decision of Substantially Equivalent on March 23, 1994. The device falls under product code DQO (Catheter, Intravascular, Diagnostic), a Class II device regulated under 21 CFR 870.1200. Target Therapeutics has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 23, 1994
- Date Received
- November 17, 1992
- 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