510(k) K951953

CARDON PHSICAL THERAPY TABLE MODEL R27630 by Cardon Rehabilitation Products, Inc. — Product Code INQ

K951953 is an FDA 510(k) premarket notification submitted by Cardon Rehabilitation Products, Inc. for the device "CARDON PHSICAL THERAPY TABLE MODEL R27630". The FDA issued a decision of Substantially Equivalent on May 31, 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
May 31, 1995
Date Received
April 26, 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