The following data is part of a premarket notification filed by Stryker Medical with the FDA for Stryker I.v. Caddy Accessory Device.
| Device ID | K920704 |
| 510k Number | K920704 |
| Device Name: | STRYKER I.V. CADDY ACCESSORY DEVICE |
| Classification | Stretcher, Wheeled |
| Applicant | STRYKER MEDICAL 6300 S. SPRINKLE RD. Kalamazoo, MI 49001 -9799 |
| Contact | James A Ahle |
| Correspondent | James A Ahle STRYKER MEDICAL 6300 S. SPRINKLE RD. Kalamazoo, MI 49001 -9799 |
| Product Code | FPO |
| CFR Regulation Number | 880.6910 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-02-18 |
| Decision Date | 1992-03-23 |