510(k) K925320

A-DEC 2145 DUO UNIT, CUSP by A-Dec, Inc. — Product Code KLC

K925320 is an FDA 510(k) premarket notification submitted by A-Dec, Inc. for the device "A-DEC 2145 DUO UNIT, CUSP". The FDA issued a decision of Substantially Equivalent on December 9, 1993. The device falls under product code KLC (Chair, Dental, With Operative Unit), a Class I device regulated under 21 CFR 872.6250. A-Dec, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 9, 1993
Date Received
October 21, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Chair, Dental, With Operative Unit
Device Class
Class I
Regulation Number
872.6250
Review Panel
DE
Submission Type