The following data is part of a premarket notification filed by Brenner Metal Prod Corp. with the FDA for Cart, Orthopedic Bed, Stryker.
| Device ID | K863685 |
| 510k Number | K863685 |
| Device Name: | CART, ORTHOPEDIC BED, STRYKER |
| Classification | Bed, Manual |
| Applicant | BRENNER METAL PROD CORP. 16 MAIN AVE. Wallington, NJ 07057 |
| Contact | Brenner, V.p. |
| Correspondent | Brenner, V.p. BRENNER METAL PROD CORP. 16 MAIN AVE. Wallington, NJ 07057 |
| Product Code | FNJ |
| CFR Regulation Number | 880.5120 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1986-09-19 |
| Decision Date | 1987-01-15 |