The following data is part of a premarket notification filed by Guardian Products Co., Inc. with the FDA for Forearm-cane.
| Device ID | K790299 |
| 510k Number | K790299 |
| Device Name: | FOREARM-CANE |
| Classification | Cane |
| Applicant | GUARDIAN PRODUCTS CO., INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | IPS |
| CFR Regulation Number | 890.3075 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-02-12 |
| Decision Date | 1979-02-21 |