510(k) K940165

ALASTIK by Unitek Corp. — Product Code ECI

K940165 is an FDA 510(k) premarket notification submitted by Unitek Corp. for the device "ALASTIK". The FDA issued a decision of Substantially Equivalent on March 7, 1994. The device falls under product code ECI (Band, Elastic, Orthodontic), a Class I device regulated under 21 CFR 872.5410. Unitek Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 7, 1994
Date Received
January 6, 1994
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Band, Elastic, Orthodontic
Device Class
Class I
Regulation Number
872.5410
Review Panel
DE
Submission Type