The following data is part of a premarket notification filed by Cozcon, Inc. with the FDA for Reflux Bed.
| Device ID | K896256 |
| 510k Number | K896256 |
| Device Name: | REFLUX BED |
| Classification | Table, Mechanical |
| Applicant | COZCON, INC. 108 NORWICH AVE. P.O. BOX 142 Colchester, CT 06415 |
| Contact | Dean Conrad |
| Correspondent | Dean Conrad COZCON, INC. 108 NORWICH AVE. P.O. BOX 142 Colchester, CT 06415 |
| Product Code | INW |
| CFR Regulation Number | 890.3750 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-10-31 |
| Decision Date | 1989-11-08 |