The following data is part of a premarket notification filed by Redman, Inc. with the FDA for Chief Sr.
| Device ID | K940919 |
| 510k Number | K940919 |
| Device Name: | CHIEF SR |
| Classification | Wheelchair, Standup |
| 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 | IPL |
| CFR Regulation Number | 890.3900 [🔎] |
| Decision | Substantially Equivalent For Some Indications (SN) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-02-24 |
| Decision Date | 1995-02-03 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00863444000308 | K940919 | 000 |