510(k) K073700
K073700 is an FDA 510(k) premarket notification submitted by St. Jude Medical, Inc. for the device "6F PROXIS SYSTEM". The FDA issued a decision of Substantially Equivalent on October 2, 2008. The device falls under product code DQY (Catheter, Percutaneous), a Class II device regulated under 21 CFR 870.1250. St. Jude Medical, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 2, 2008
- Date Received
- December 31, 2007
- Clearance Type
- Traditional
- 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