510(k) K950363

CARDONPHYSICAL THERAPY TABLE R27110 by Cardon Rehabilitation Products, Inc. — Product Code INQ

K950363 is an FDA 510(k) premarket notification submitted by Cardon Rehabilitation Products, Inc. for the device "CARDONPHYSICAL THERAPY TABLE R27110". The FDA issued a decision of Substantially Equivalent on February 10, 1995. 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 10, 1995
Date Received
January 30, 1995
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