The following data is part of a premarket notification filed by Sage Products, Inc. with the FDA for Arm Board W/i.v Covering.
| Device ID | K823412 |
| 510k Number | K823412 |
| Device Name: | ARM BOARD W/I.V COVERING |
| Classification | Board, Arm (with Cover), Sterile |
| Applicant | SAGE PRODUCTS, INC. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | BTX |
| CFR Regulation Number | 878.3910 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-11-15 |
| Decision Date | 1982-12-15 |