The following data is part of a premarket notification filed by Cardon Rehabilitation Products, Inc. with the FDA for Cardon Physical Therapy Tables Models R28591 & R28592.
| Device ID | K951906 |
| 510k Number | K951906 |
| Device Name: | CARDON PHYSICAL THERAPY TABLES MODELS R28591 & R28592 |
| Classification | Table, Powered |
| Applicant | CARDON REHABILITATION PRODUCTS, INC. 16617 KILLDEER DR. Rockville, MD 20855 |
| Contact | Glenn E Conklin |
| Correspondent | Glenn E Conklin CARDON REHABILITATION PRODUCTS, INC. 16617 KILLDEER DR. Rockville, MD 20855 |
| Product Code | INQ |
| CFR Regulation Number | 890.3760 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-04-24 |
| Decision Date | 1995-06-15 |