Oxoid , Ltd.
Oxoid , Ltd. appears in FDA public data with 0 recalls, 36 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on March 14, 2007.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 36
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K070262 | ERTAPENEM ANTIMICROBIAL SUSCEPTIBILITY TEST DISC | March 14, 2007 |
| K060286 | TIGECYCLINE ANTIMICROBIAL SUSCEPTIBILITY TEST DISC | March 17, 2006 |
| K042157 | DAPTOMYCIN ANTIMICROBIAL SUSCEPTIBILITY TEST DISC | September 14, 2004 |
| K011710 | OXOID PBP2 1 LATEX AGGLUTINATION TEST | April 2, 2002 |
| K012588 | OXOID PYLORI TEST KIT, MODEL DR0130M | December 10, 2001 |
| K010537 | LINEZOLID ANTIMICROBIAL SUSCEPTIBILITY TEST DISC | April 24, 2001 |
| K010536 | MOXIFLOXACIN ANTIMICROBIAL SUSCEPTIBILITY TEST DISC | April 24, 2001 |
| K000930 | GATIFLOXACIN ANTIMICROBIAL SUSCEPTIBILITY TEST DISC | May 22, 2000 |
| K000928 | QUINUPRISTIN/DALFOPRISTIN ANTIMICROBIAL SUSCEPTIBILITY TEST DISC | May 15, 2000 |
| K993401 | DRYSPOT E.COLI 0157 KIT | February 28, 2000 |
| K984513 | TROVAFLOXACIN ANTIMICROBIAL SUSCEPTIBILITY TEST DISC | April 2, 1999 |
| K984608 | GENTAMICIN ANTIMICROBIAL SUSCEPTIBILITY TEST DISC | March 9, 1999 |
| K982634 | DRYSPOT INFECTIOUS MONONUCLEOSIS KIT | January 28, 1999 |
| K984036 | NETILMICIN ANTIMICROBIAL SUSCEPTIBILITY TEST DISC | January 13, 1999 |
| K983718 | MEROPENEM ANTIMICROBIAL SUSCEPTIBILITY TEST DISC | December 11, 1998 |
| K982523 | SULFISOXAZOLE ANTIMICROBIAL SUSCEPTIBILITY TEST DISC | September 9, 1998 |
| K982520 | CEFONICID ANTIMICROBIAL SUSCEPTIBILITY TEST DISC | September 9, 1998 |
| K982526 | SPARFLOXACIN ANTIMICROBIAL SUSCEPTIBILITY TEST DISC | September 9, 1998 |
| K982519 | LEVOFLOXACIN ANTIMICROBIAL SUSCEPTIBILITY TEST DISC | September 9, 1998 |
| K982528 | NAFCILLIN ANTIMICROBIAL SUSCEPTIBILITY TEST DISC | September 9, 1998 |