510(k) K964859
K964859 is an FDA 510(k) premarket notification submitted by Scimed Life Systems, Inc. for the device "SCIMED 5 FRENCH IMPULSE ANGIOGRAPHIC CATHETERS". The FDA issued a decision of Substantially Equivalent on February 10, 1997. The device falls under product code DQO (Catheter, Intravascular, Diagnostic), a Class II device regulated under 21 CFR 870.1200. Scimed Life Systems, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 10, 1997
- Date Received
- December 4, 1996
- 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