Company ยท US
Cottrell, Ltd.
FDA 510(k) clearances and medical device recalls filed under this name, 1990 to 1999. Name variants (Inc, Corp, punctuation) are merged.
9510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Sep 13, 1999 | K972708 | ENDO-SPOR PLUS / HYPROCIDE Cottrell, Ltd. | MED |
| May 18, 1998 | K970726 | VAPOCIDE Cottrell, Ltd. | MED |
| Apr 4, 1996 | K960089 | PROCHEK G GLUTARALDEHYDE CONCENTRATION LEVEL INDICATOR Cottrell, Ltd. | JOJ |
| Aug 7, 1995 | K952241 | PROTOUCH OVERGLOVE Cottrell, Ltd. | MMP |
| Jul 31, 1995 | K952234 | BARRIER ALL FILM Cottrell, Ltd. | EFS |
| Jul 3, 1995 | K932922 | PROCIDE 14 N.S., OMNICIDE/LIQUID & PLUS LIQ ACTIVATOR Cottrell, Ltd. | MED |
| Jun 20, 1995 | K951983 | IMNI-II Cottrell, Ltd. | LRJ |
| Mar 6, 1995 | K945575 | PRO BARRIER(TM) TUBE SOX(TM) Cottrell, Ltd. | MMN |
| Apr 4, 1990 | K893802 | PROVIEW SELF-SEALING STERILIZATION POUCH Cottrell, Ltd. | KCT |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||