Company ยท US
M.A. Bioproducts
FDA 510(k) clearances and medical device recalls filed under this name, 1980 to 1983. Name variants (Inc, Corp, punctuation) are merged.
12510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
| Code | Device | Records |
|---|---|---|
| GOL | Antigen, Ha (Including Ha Control), Rubella | 1 |
| KIT | Media And Components, Synthetic Cell And Tissue Culture | 1 |
| LCS | Radioimmunoassay, Digoxin (125-I) | 1 |
| LFY | Enzyme Linked Immunoabsorbent Assay, Varicella-Zoster | 1 |
| LFZ | Enzyme Linked Immunoabsorbent Assay, Cytomegalovirus | 1 |
| LGC | Enzyme Linked Immunoabsorbent Assay, Herpes Simplex Virus, Non-Specific | 1 |
| LGD | Enzyme Linked Immunoabsorbent Assay, Toxoplasma Gondii | 1 |
| LJB | Enzyme Linked Immunoabsorbent Assay, Rubeola Igg | 1 |
| LJC | Enzyme Linked Immunoabsorbent Assay, (Chlamydiae Group) | 1 |
| LJY | Enzyme Linked Immunoabsorbent Assay, Mumps Virus | 1 |
| LJZ | Enzyme Linked Immunoabsorbent Assay, Mycoplasma Spp. | 1 |
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Jul 26, 1983 | K822883 | HERPELISA KIT M.A. Bioproducts | LGC |
| May 25, 1983 | K823804 | MYCOPLASMELISA TEST KIT M.A. Bioproducts | LJZ |
| May 13, 1983 | K830045 | MUMPSELISA TEST KIT M.A. Bioproducts | LJY |
| May 9, 1983 | K830615 | CYTOMEGELISA STAT M.A. Bioproducts | LFZ |
| May 5, 1983 | K823805 | VARICELISA TEST KIT M.A. Bioproducts | LFY |
| Aug 3, 1982 | K821967 | CHLAMYDELISA TEST KIT M.A. Bioproducts | LJC |
| Jul 30, 1982 | K821762 | MEASELISA TEST KIT M.A. Bioproducts | LJB |
| Jan 26, 1982 | K813221 | TOXOELISA TEST KIT M.A. Bioproducts | LGD |
| Oct 23, 1981 | K812531 | CELL CULTURE REAGENTS M.A. Bioproducts | KIT |
| Sep 23, 1981 | K812123 | CYTOMEGELISA TEST KIT M.A. Bioproducts | |
| Dec 18, 1980 | K802508 | RUBELISA IGM TEST KIT M.A. Bioproducts | GOL |
| Jul 14, 1980 | K801490 | DIGOXIN EIA KIT M.A. Bioproducts | LCS |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||