The following data is part of a premarket notification filed by J. T. Posey Co. with the FDA for Posey Sitter.
| Device ID | K920206 |
| 510k Number | K920206 |
| Device Name: | POSEY SITTER |
| Classification | Monitor, Bed Patient |
| Applicant | J. T. POSEY CO. 5635 PECK RD. Arcadia, CA 91006 |
| Contact | Ernest Posey |
| Correspondent | Ernest Posey J. T. POSEY CO. 5635 PECK RD. Arcadia, CA 91006 |
| Product Code | KMI |
| CFR Regulation Number | 880.2400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-01-16 |
| Decision Date | 1992-05-14 |