510(k) K094062
K094062 is an FDA 510(k) premarket notification submitted by Cardiosolutions, Inc. for the device "PERCU-PRO GUIDEWIRE". The FDA issued a decision of Substantially Equivalent on September 27, 2010. The device falls under product code DQX (Wire, Guide, Catheter), a Class II device regulated under 21 CFR 870.1330. Cardiosolutions, Inc. has at least 4 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 27, 2010
- Date Received
- December 31, 2009
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Wire, Guide, Catheter
- Device Class
- Class II
- Regulation Number
- 870.1330
- Review Panel
- CV
- Submission Type