The following data is part of a premarket notification filed by Medmark, Inc. with the FDA for Model #520/525 Ed/recovery Stretcher.
| Device ID | K894987 |
| 510k Number | K894987 |
| Device Name: | MODEL #520/525 ED/RECOVERY STRETCHER |
| Classification | Table, Mechanical |
| Applicant | MEDMARK, INC. Versailles, OH 45380 |
| Contact | John Oldiges |
| Correspondent | John Oldiges MEDMARK, INC. Versailles, OH 45380 |
| Product Code | INW |
| CFR Regulation Number | 890.3750 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-08-08 |
| Decision Date | 1989-09-05 |