510(k) K010692
K010692 is an FDA 510(k) premarket notification submitted by Spintech, Inc. for the device "THE WAND PLUS COMPUTER CONTROLLED ANESTHETIC DELIVERY SYSTEM". The FDA issued a decision of Substantially Equivalent on June 29, 2001. The device falls under product code FMF (Syringe, Piston), a Class II device regulated under 21 CFR 880.5860. Spintech, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 29, 2001
- Date Received
- March 8, 2001
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Syringe, Piston
- Device Class
- Class II
- Regulation Number
- 880.5860
- Review Panel
- HO
- Submission Type