The following data is part of a premarket notification filed by Cardon Rehabilitation Products, Inc. with the FDA for Cardon Physical Therapy Table Model R28598.
| Device ID | K960332 |
| 510k Number | K960332 |
| Device Name: | CARDON PHYSICAL THERAPY TABLE MODEL R28598 |
| Classification | Table, Powered |
| Applicant | CARDON REHABILITATION PRODUCTS, INC. 2045 NIAGARA FALLS BLVD., UNIT #5, P.O. BOX 237 Niagara Falls, NY 14304 -0237 |
| Contact | C.e. Cardon |
| Correspondent | C.e. Cardon CARDON REHABILITATION PRODUCTS, INC. 2045 NIAGARA FALLS BLVD., UNIT #5, P.O. BOX 237 Niagara Falls, NY 14304 -0237 |
| Product Code | INQ |
| CFR Regulation Number | 890.3760 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-01-24 |
| Decision Date | 1996-02-13 |