Cottrell, Ltd.
Cottrell, Ltd. appears in FDA public data with 0 recalls, 9 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on September 13, 1999.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 9
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K972708 | ENDO-SPOR PLUS / HYPROCIDE | September 13, 1999 |
| K970726 | VAPOCIDE | May 18, 1998 |
| K960089 | PROCHEK G GLUTARALDEHYDE CONCENTRATION LEVEL INDICATOR | April 4, 1996 |
| K952241 | PROTOUCH OVERGLOVE | August 7, 1995 |
| K952234 | BARRIER ALL FILM | July 31, 1995 |
| K932922 | PROCIDE 14 N.S., OMNICIDE/LIQUID & PLUS LIQ ACTIVATOR | July 3, 1995 |
| K951983 | IMNI-II | June 20, 1995 |
| K945575 | PRO BARRIER(TM) TUBE SOX(TM) | March 6, 1995 |
| K893802 | PROVIEW SELF-SEALING STERILIZATION POUCH | April 4, 1990 |