FDA 510(k) Applications Submitted by C. E CARDON

FDA 510(k) Number Submission Date Device Name Applicant
K960334 01/24/1996 CARDON PHYSICAL THERAPY TABLE MODEL R27116 CARDON REHABILITATION PRODUCTS, INC.
K960332 01/24/1996 CARDON PHYSICAL THERAPY TABLE MODEL R28598 CARDON REHABILITATION PRODUCTS, INC.


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