The following data is part of a premarket notification filed by Cardon Rehabilitation Products, Inc. with the FDA for Cardon Phsical Therapy Table Model R27630.
| Device ID | K951953 |
| 510k Number | K951953 |
| Device Name: | CARDON PHSICAL THERAPY TABLE MODEL R27630 |
| 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 | 1995-04-26 |
| Decision Date | 1995-05-31 |