FDA 510(k) Applications Submitted by Donna T. Link
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K191442 |
05/30/2019 |
Campylobacter Chek |
Techlab, Inc. |
| K191456 |
05/31/2019 |
Campylobacter Quik Chek |
Techlab, Inc |
| K121364 |
05/07/2012 |
SHIGA TOXIN QUIK CHEK |
TECHLAB INC., CORPORATE RESEARCH CENTER |
| K121411 |
05/11/2012 |
SHIGA TOXIN CHEK |
TECHLAB INC., CORPORATE RESEARCH CENTER |
| K103673 |
12/16/2010 |
GIARDIA/ CRYPTOSPORIDIUM QUIK CHEK |
TECHLAB INC., CORPORATE RESEARCH CENTER |
| K170728 |
03/09/2017 |
E. HISTOLYTICA QUIK CHEK |
TECHLAB, Inc. |
| K171078 |
04/11/2017 |
TRI-COMBO PARASITE SCREEN |
Techlab, Inc. |
| K181379 |
05/24/2018 |
H. PYLORI QUIK CHEK |
TECHLAB, Inc. |
| K181400 |
05/29/2018 |
H. PYLORI CHEKÖ |
TECHLAB, Inc. |
| K173217 |
10/03/2017 |
CAMPYLOBACTER QUIK CHEK |
Techlab, Inc. |
| K173219 |
10/03/2017 |
CAMPYLOBACTER CHEK |
Techlab, Inc. |
|
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