Lmd Laboratories
Lmd Laboratories appears in FDA public data with 0 recalls, 12 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on June 7, 1996.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 12
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K955345 | LMD CRYPTOSPORIDIUM ANTIGEN DETECTION | June 7, 1996 |
| K942705 | E. COLI 0157 ELISA STOOL ASSAY | September 27, 1995 |
| K944871 | LMD GIARDIA ANTIGEN DETECTION ASSAY | June 22, 1995 |
| K905598 | CRYPTOSPORIDIUM ANTIGEN DETECTION | September 5, 1991 |
| K904613 | TRICHINELLA SEROLOGY MICROTITER ELISA | March 21, 1991 |
| K900780 | CYSTICERCOSIS SEROLOGICAL REAGENTS | October 4, 1990 |
| K890003 | GIARDIA STOOL ANTIGEN TEST KIT | March 14, 1989 |
| K883720 | TREND(R) EMERGE(TM) TOXOPLASMA IGG ELISA | January 24, 1989 |
| K870318 | AMEBIASIS ELISA TEST KIT | August 11, 1987 |
| K854230 | MEBIASIS AGAR GEL DIFFUSION KIT | November 12, 1985 |
| K854017 | ENTAMOEBA HISTOLYTICA-POSITIVE CONTROL(RABBIT) | October 22, 1985 |
| K844141 | ENTAMOEBA HISTOLYTICA HK-9 ANTIGEN (AXENIC) | December 6, 1984 |