Redman, Inc.
Bloomington, MN, US
Redman, Inc. appears in FDA device records in Bloomington, MN. FDA records list 16 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 16
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 16 510(k) clearances for Redman, Inc. between 1987 and 1995. The busiest year on record is 1987, with 9. The most recent is 1995, with 7.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1987 | 9 |
| 1995 | 7 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K940920 | ROAD SAVAGE | ITI | Substantially Equivalent for Some Indications | |
| K940919 | CHIEF SR | IPL | Substantially Equivalent for Some Indications | |
| K940852 | CHIEF STANDUP WHEELCHAIR | IPL | Substantially Equivalent for Some Indications | |
| K940851 | RED PACK MANLUAL POWER WHEELCHAIR CONVERSION KIT | ITI | Substantially Equivalent for Some Indications | |
| K935751 | GERONIMO PR | ITI | Substantially Equivalent for Some Indications | |
| K935750 | GERONIMO | ITI | Substantially Equivalent for Some Indications | |
| K935749 | ROAD WARRIOR | ITI | Substantially Equivalent for Some Indications | |
| K870298 | REDMAN ACCESSORIES | KNO | Substantially Equivalent | |
| K870299 | REDMAN UPHOLSTERY SERIES FOR WHEELCHAIRS | KNN | Substantially Equivalent | |
| K870297 | DAKOTA MODEL 102C WHEELCHAIR | ITI | Substantially Equivalent | |
| K870296 | MOHAVE MODEL 102W WHEELCHAIR | IOR | Substantially Equivalent | |
| K870295 | SIOUX MODEL 102ALW WHEELCHAIR | IOR | Substantially Equivalent | |
| K870294 | CROW MODEL 106A WHEELCHAIR | IOR | Substantially Equivalent | |
| K870293 | NAVAJO MODEL 103A WHEELCHAIR | IOR | Substantially Equivalent | |
| K870292 | CHEYENNE MODEL 107A WHEELCHAIR | IOR | Substantially Equivalent | |
| K870291 | CHEROKEE MODEL 102A WHEELCHAIR | IOR | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
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Data as of , FDA export datePage updated Source: openFDA, public domain
