510(k) K960336

CARDON PHYSICAL THERAPY TABLE MODEL R27645 by Cardon Rehabilitation Products, Inc. — Product Code INQ

K960336 is an FDA 510(k) premarket notification submitted by Cardon Rehabilitation Products, Inc. for the device "CARDON PHYSICAL THERAPY TABLE MODEL R27645". The FDA issued a decision of Substantially Equivalent on February 13, 1996. The device falls under product code INQ (Table, Powered), a Class I device regulated under 21 CFR 890.3760. Cardon Rehabilitation Products, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 13, 1996
Date Received
January 24, 1996
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Table, Powered
Device Class
Class I
Regulation Number
890.3760
Review Panel
PM
Submission Type