510(k) K850009
K850009 is an FDA 510(k) premarket notification submitted by Vas-Cath of Canada , Ltd. for the device "EVANS, VAS-CATH EPIDURAL NEEDLE & CATHETER". The FDA issued a decision of Substantially Equivalent on May 13, 1985. The device falls under product code BSO (Catheter, Conduction, Anesthetic), a Class II device regulated under 21 CFR 868.5120. Vas-Cath of Canada , Ltd. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 13, 1985
- Date Received
- January 2, 1985
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Catheter, Conduction, Anesthetic
- Device Class
- Class II
- Regulation Number
- 868.5120
- Review Panel
- AN
- Submission Type