FDA 510(k) Applications Submitted by SDI DIAGNOSTICS, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K150515 |
03/02/2015 |
IQSense Flow Sensor Mouthpiece |
SDI DIAGNOSTICS, INC. |
| K061571 |
06/06/2006 |
ASTRA 300 |
SDI DIAGNOSTICS, INC. |
| K092813 |
09/14/2009 |
ASTRASONIC SPIROMETER, MODEL 29-8000 |
SDI DIAGNOSTICS, INC. |
| K062913 |
09/27/2006 |
ASTRAGUARD PULMONARY FUNCTION FILTER |
SDI DIAGNOSTICS, INC. |
| K990962 |
03/22/1999 |
FLOSENSE, MODEL 29-8010 |
SDI DIAGNOSTICS, INC. |
| K011470 |
05/14/2001 |
SDI SB OFFICE, MODEL 29- |
SDI DIAGNOSTICS, INC. |
| K031643 |
05/27/2003 |
SPIROTEL, MODEL 29-1020 |
SDI DIAGNOSTICS, INC. |
| K013812 |
11/15/2001 |
SPIROLAB II, MODEL 29 |
SDI DIAGNOSTICS, INC. |
| K033939 |
12/15/2003 |
FLOSENSE II, MODEL 29-8040 |
SDI DIAGNOSTICS, INC. |
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