Techlab, Inc.
FDA 510(k) & PMA Approved Devices — 36 products
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Total Devices36
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K191442 | Campylobacter Chek | LQP | 2019-06-20 | View |
| 510(k) | K191456 | Campylobacter Quik Chek | LQP | 2019-06-20 | View |
| 510(k) | K181400 | H. PYLORI CHEK™ | LYR | 2018-08-21 | View |
| 510(k) | K181379 | H. PYLORI QUIK CHEK | LYR | 2018-08-21 | View |
| 510(k) | K173217 | CAMPYLOBACTER QUIK CHEK | LQP | 2018-01-22 | View |
| 510(k) | K173219 | CAMPYLOBACTER CHEK | LQP | 2018-01-22 | View |
| 510(k) | K171078 | TRI-COMBO PARASITE SCREEN | MHJ | 2017-07-10 | View |
| 510(k) | K170728 | E. HISTOLYTICA QUIK CHEK | KHW | 2017-06-07 | View |
| 510(k) | K082499 | C. DIFF QUIK CHEK COMPLETE | LLH | 2009-03-26 | View |
| 510(k) | K053572 | C. DIFF QUIK CHEK | MCB | 2006-04-26 | View |
| 510(k) | K051927 | TECHLAB ASCA-CHEK | NBT | 2006-04-06 | View |
| 510(k) | K051929 | GIARDIA/CRYPTOSPORIDIUM CHEK | MHJ | 2005-11-17 | View |
| 510(k) | K052932 | CRYPTOSPORIDIUM II | MHJ | 2005-11-04 | View |
| 510(k) | K050891 | TOX A/B QUICK CHEK | LLH | 2005-07-25 | View |
| 510(k) | K042071 | IBD-SCAN | DEG | 2004-10-20 | View |
| 510(k) | K033274 | GIARDIA II | MHI | 2003-11-04 | View |
| 510(k) | K030992 | C. DIFF CHEK - 60 | LLH | 2003-07-11 | View |
| 510(k) | K030991 | C. DIFF CHEK - 30 | LLH | 2003-07-11 | View |
| 510(k) | K030404 | C. DIFFICILE TOX A/B II | LLH | 2003-04-24 | View |
| 510(k) | K030704 | IBD-QUIK CHEK | DEG | 2003-04-21 | View |
No matching devices.
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