510(k) K772300

DENTAL CHAIR, VANGUARD by Ritter Co. — Product Code KLC

K772300 is an FDA 510(k) premarket notification submitted by Ritter Co. for the device "DENTAL CHAIR, VANGUARD". The FDA issued a decision of Substantially Equivalent on January 3, 1978. The device falls under product code KLC (Chair, Dental, With Operative Unit), a Class I device regulated under 21 CFR 872.6250. Ritter Co. has at least 9 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 3, 1978
Date Received
December 14, 1977
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