510(k) K822013

NAGASHIMA SN AUTOMATIC TREATMENT CHAIR by Kelleher Corp. — Product Code GBB

K822013 is an FDA 510(k) premarket notification submitted by Kelleher Corp. for the device "NAGASHIMA SN AUTOMATIC TREATMENT CHAIR". The FDA issued a decision of Substantially Equivalent on July 28, 1982. The device falls under product code GBB (Chair, Surgical, Ac-Powered), a Class I device regulated under 21 CFR 878.4960. Kelleher Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 28, 1982
Date Received
July 8, 1982
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Chair, Surgical, Ac-Powered
Device Class
Class I
Regulation Number
878.4960
Review Panel
SU
Submission Type