510(k) K994229
K994229 is an FDA 510(k) premarket notification submitted by Advanced Cardiovascular Systems, Inc. for the device "VERIPATH PERIPHERAL GUIDING CATHETER". The FDA issued a decision of Substantially Equivalent on February 25, 2000. The device falls under product code DQY (Catheter, Percutaneous), a Class II device regulated under 21 CFR 870.1250. Advanced Cardiovascular Systems, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 25, 2000
- Date Received
- December 16, 1999
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Catheter, Percutaneous
- Device Class
- Class II
- Regulation Number
- 870.1250
- Review Panel
- CV
- Submission Type