510(k) K961648

THE WAND by Spintech, Inc. — Product Code EJI

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