The following data is part of a premarket notification filed by Redman, Inc. with the FDA for Geronimo Pr.
| Device ID | K935751 |
| 510k Number | K935751 |
| Device Name: | GERONIMO PR |
| Classification | Wheelchair, Powered |
| Applicant | REDMAN, INC. 945 EAST OHIO, SUITE #4 Tucson, AZ 85714 |
| Contact | Don Redman |
| Correspondent | Don Redman REDMAN, INC. 945 EAST OHIO, SUITE #4 Tucson, AZ 85714 |
| Product Code | ITI |
| CFR Regulation Number | 890.3860 [🔎] |
| Decision | Substantially Equivalent For Some Indications (SN) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-11-26 |
| Decision Date | 1995-02-03 |