FDA 510(k) Applications Submitted by M J TAYLOR
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K980574 |
02/17/1998 |
AURAFLEX TSH-3 200 TEST PACK MODEL NUMBER 80600, AURAFLEX TSH-3 CALIBRATOR PACK MODEL NUMBER NUMBER 80601 AURAFLEX DIL0 |
ALFA BIOTECH (UK) LTD. |
| K974505 |
12/01/1997 |
AURAFLEX FERRITIN 200 TEST PACK 80500, AURAFLEX FERRITIN CALIBRATOR PACK 80501 |
ALFA BIOTECH (UK) LTD. |
| K974027 |
10/23/1997 |
AURAFLEX FT3 150 TEST PACK, AURAFLEX FT3 CALIBRATOR PACK |
ALFA BIOTECH (UK) LTD. |
| K161937 |
07/14/2016 |
CuattroDR |
Cuattro, LLC |
| K993812 |
11/10/1999 |
CVM TRANSPORT, MODEL R96,VIRAL TRANSPORT, MODEL R99, CVM TRANSPORT KIT, MODEL R96 K, VIRAL TRANSPORT KIT, MODEL R99 K |
HARDY DIAGNOSTICS |
| K955451 |
11/29/1995 |
CVM TRANSPORT |
HARDY DIAGNOSTICS |
| K202837 |
09/25/2020 |
GoSpiro |
Monitored Therapeutics, Inc. |
|
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