The following data is part of a premarket notification filed by Stryker Corp. with the FDA for Stryker Powered Wheeled Stretcher.
| Device ID | K022309 |
| 510k Number | K022309 |
| Device Name: | STRYKER POWERED WHEELED STRETCHER |
| Classification | Stretcher, Wheeled, Powered |
| Applicant | STRYKER CORP. 1730 PENNSYLVANIA AVENUE N.W. Washington, DC 20006 -4706 |
| Contact | Lynette Gabriel |
| Correspondent | Lynette Gabriel STRYKER CORP. 1730 PENNSYLVANIA AVENUE N.W. Washington, DC 20006 -4706 |
| Product Code | INK |
| CFR Regulation Number | 890.3690 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2002-07-16 |
| Decision Date | 2002-11-08 |
| Summary: | summary |