The following data is part of a premarket notification filed by Redman, Inc. with the FDA for Redman Accessories.
| Device ID | K870298 |
| 510k Number | K870298 |
| Device Name: | REDMAN ACCESSORIES |
| Classification | Accessories, Wheelchair |
| Applicant | REDMAN, INC. 9340 COLORADO AVE. Bloomington, MN 55438 |
| Contact | Michael R Miller |
| Correspondent | Michael R Miller REDMAN, INC. 9340 COLORADO AVE. Bloomington, MN 55438 |
| Product Code | KNO |
| CFR Regulation Number | 890.3910 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-01-28 |
| Decision Date | 1987-02-26 |