510(k) K923999

ALASTIK NS by Unitek Corp. — Product Code ECI

K923999 is an FDA 510(k) premarket notification submitted by Unitek Corp. for the device "ALASTIK NS". The FDA issued a decision of Substantially Equivalent on June 24, 1993. 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
June 24, 1993
Date Received
August 10, 1992
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