Cottrell, Ltd.
FDA 510(k) & PMA Approved Devices — 9 products
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Total Devices9
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K972708 | ENDO-SPOR PLUS / HYPROCIDE | MED | 1999-09-13 | View |
| 510(k) | K970726 | VAPOCIDE | MED | 1998-05-18 | View |
| 510(k) | K960089 | PROCHEK G GLUTARALDEHYDE CONCENTRATION LEVEL INDICATOR | JOJ | 1996-04-04 | View |
| 510(k) | K952241 | PROTOUCH OVERGLOVE | MMP | 1995-08-07 | View |
| 510(k) | K952234 | BARRIER ALL FILM | EFS | 1995-07-31 | View |
| 510(k) | K932922 | PROCIDE 14 N.S., OMNICIDE/LIQUID & PLUS LIQ ACTIVATOR | MED | 1995-07-03 | View |
| 510(k) | K951983 | IMNI-II | LRJ | 1995-06-20 | View |
| 510(k) | K945575 | PRO BARRIER(TM) TUBE SOX(TM) | MMN | 1995-03-06 | View |
| 510(k) | K893802 | PROVIEW SELF-SEALING STERILIZATION POUCH | KCT | 1990-04-04 | View |
No matching devices.
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