510(k) K920016

IMPROVED DENTAL CHAIR by Den-Tal-Ez Mfg Co., Inc. — Product Code KLC

K920016 is an FDA 510(k) premarket notification submitted by Den-Tal-Ez Mfg Co., Inc. for the device "IMPROVED DENTAL CHAIR". The FDA issued a decision of Substantially Equivalent on March 2, 1992. The device falls under product code KLC (Chair, Dental, With Operative Unit), a Class I device regulated under 21 CFR 872.6250. Den-Tal-Ez Mfg Co., Inc. has at least 6 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 2, 1992
Date Received
January 2, 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