The following data is part of a premarket notification filed by Cardon Rehabilitation Products, Inc. with the FDA for Cardon Physical Therapy Table Model R27645.
Device ID | K960336 |
510k Number | K960336 |
Device Name: | CARDON PHYSICAL THERAPY TABLE MODEL R27645 |
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 |