The following data is part of a premarket notification filed by Cambridge Technologies, Inc. with the FDA for Stretcher, Wheeled, Mechanical.
| Device ID | K873181 |
| 510k Number | K873181 |
| Device Name: | STRETCHER, WHEELED, MECHANICAL |
| Classification | Stretcher, Wheeled |
| Applicant | CAMBRIDGE TECHNOLOGIES, INC. 300 MUIR ST. Cambridge, MD 21613 |
| Contact | Donald Holdt |
| Correspondent | Donald Holdt CAMBRIDGE TECHNOLOGIES, INC. 300 MUIR ST. Cambridge, MD 21613 |
| Product Code | FPO |
| CFR Regulation Number | 880.6910 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-08-12 |
| Decision Date | 1987-10-09 |