510(k) K992819

WAND PLUS by Spintech, Inc. — Product Code EJI

K992819 is an FDA 510(k) premarket notification submitted by Spintech, Inc. for the device "WAND PLUS". The FDA issued a decision of Substantially Equivalent on May 11, 2000. 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
May 11, 2000
Date Received
August 20, 1999
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