The following data is part of a premarket notification filed by Stryker Corp. with the FDA for Stryker Powered Stretcher.
| Device ID | K942948 |
| 510k Number | K942948 |
| Device Name: | STRYKER POWERED STRETCHER |
| Classification | Stretcher, Wheeled |
| Applicant | STRYKER CORP. MEDICAL DIV. 6300 SPRINKLE RD. Kalamazoo, MI 49001 -6197 |
| Contact | Richard Bartow |
| Correspondent | Richard Bartow STRYKER CORP. MEDICAL DIV. 6300 SPRINKLE RD. Kalamazoo, MI 49001 -6197 |
| Product Code | FPO |
| CFR Regulation Number | 880.6910 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-06-23 |
| Decision Date | 1995-01-24 |