510(k) K760322

CHAIR, ATTACHED INSTRUMENT DEL. SYS. by The S. S. White Co. — Product Code KLC

K760322 is an FDA 510(k) premarket notification submitted by The S. S. White Co. for the device "CHAIR, ATTACHED INSTRUMENT DEL. SYS.". The FDA issued a decision of Substantially Equivalent on August 3, 1976. The device falls under product code KLC (Chair, Dental, With Operative Unit), a Class I device regulated under 21 CFR 872.6250. The S. S. White Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 3, 1976
Date Received
July 26, 1976
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