FDA 510(k) Applications Submitted by JUDY BURTON
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K100246 |
01/27/2010 |
MAX-IF1000 |
BIO PROTECH, INC. |
| K100794 |
03/22/2010 |
FLUORCANASITE DENTAL CERAMIC |
DR SARAH POLLINGTON |
| K100950 |
04/06/2010 |
VENNER PNEUX P.Y. (TM) TRACHEOSTOMY TUBE |
VENNER MEDICAL (SINGAPORE) PTE LTD |
| K091248 |
04/28/2009 |
MAXEMS, MODELS 1000 AND 2000 |
BIO PROTECH, INC. |
| K111270 |
05/03/2011 |
REUSABLE STIMULATING ELECTRODES |
BIO PROTECH, INC. |
| K092761 |
09/09/2009 |
PROPLATE, MODELS 9641C, 9641F, P9641C, P9641F, 9642C, 9642F AND P9642C |
BIO PROTECH, INC. |
| K093135 |
10/05/2009 |
VENNER PNEUX P.Y. (TM) TRACHEOSTOMY TUBE AND ENDO TRACHEAL TUBE |
VENNER MEDICAL (SINGAPORE) PTE LTD |
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