510(k) K951906

CARDON PHYSICAL THERAPY TABLES MODELS R28591 & R28592 by Cardon Rehabilitation Products, Inc. — Product Code INQ

K951906 is an FDA 510(k) premarket notification submitted by Cardon Rehabilitation Products, Inc. for the device "CARDON PHYSICAL THERAPY TABLES MODELS R28591 & R28592". The FDA issued a decision of Substantially Equivalent on June 15, 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
June 15, 1995
Date Received
April 24, 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