Midwest Reprocessing Center, LLC
FDA 510(k) & PMA Approved Devices — 4 products
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Total Devices4
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K111007 | MIDWEST REPROCESSING CENTER REPROCESSED LNCS SESSORS; MIDWEST REPROCESSING CENTER REPROCESSED OXIMAX SENSORS; MIDWEST RE | NMD | 2011-06-08 | View |
| 510(k) | K101280 | MIDWESTERN REPROCESSING CENTER REPROCESSED PULSE OXIMETER PROBE | NLF | 2010-10-07 | View |
| 510(k) | K101330 | MIDWEST REPROCESSING CENTER REPROCESSED SCD EXPRESS SLEEVES/ FOOT CUFFS, MIDWEST REPROCESSING CENTER REPROCESSED ALP SLE | JOW | 2010-08-27 | View |
| 510(k) | K101702 | MIDWEST REPROCESSING CENTER REPROCESSED VENODYNE SLEEVES/FOOT CUFFS | JOW | 2010-08-27 | View |
No matching devices.
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