The following data is part of a premarket notification filed by Winco, Inc. with the FDA for Caremor Cliner.
| Device ID | K941569 |
| 510k Number | K941569 |
| Device Name: | CAREMOR CLINER |
| Classification | Chair, With Casters |
| Applicant | WINCO, INC. 5516 S.W. FIRST LN. Ocala, FL 34474 |
| Contact | Don R Frank |
| Correspondent | Don R Frank WINCO, INC. 5516 S.W. FIRST LN. Ocala, FL 34474 |
| Product Code | INM |
| CFR Regulation Number | 890.3100 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-03-31 |
| Decision Date | 1994-04-26 |