510(k) K822251

EXAMINATION & TREATMENT CHAIRS by Kelleher Corp. — Product Code GBB

K822251 is an FDA 510(k) premarket notification submitted by Kelleher Corp. for the device "EXAMINATION & TREATMENT CHAIRS". The FDA issued a decision of Substantially Equivalent on August 27, 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
August 27, 1982
Date Received
July 29, 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