510(k) K961648
K961648 is an FDA 510(k) premarket notification submitted by Spintech, Inc. for the device "THE WAND". The FDA issued a decision of Substantially Equivalent on July 5, 1996. The device falls under product code EJI (Syringe, Cartridge), a Class II device regulated under 21 CFR 872.6770. Spintech, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 5, 1996
- Date Received
- April 29, 1996
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Syringe, Cartridge
- Device Class
- Class II
- Regulation Number
- 872.6770
- Review Panel
- DE
- Submission Type