The following data is part of a premarket notification filed by Dyna Corp. with the FDA for Hare Emergency Stretcher.
| Device ID | K900670 |
| 510k Number | K900670 |
| Device Name: | HARE EMERGENCY STRETCHER |
| Classification | Stretcher, Hand-carried |
| Applicant | DYNA CORP. 6300 YARROW DR. Carlsbad, CA 92009 -1597 |
| Contact | R. A Yaeger |
| Correspondent | R. A Yaeger DYNA CORP. 6300 YARROW DR. Carlsbad, CA 92009 -1597 |
| Product Code | FPP |
| CFR Regulation Number | 880.6900 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-02-13 |
| Decision Date | 1990-04-23 |