FDA 510(k) Applications Submitted by PROGENY, INC.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K020070 |
01/09/2002 |
JB-70 INTRAORAL X-RAY SYSTEM, MODELS 30-A0001/A0002 |
PROGENY, INC. |
K090079 |
01/12/2009 |
VIVID, MODELS 40-A0001, 40-A0004, 40-A0006 |
PROGENY, INC. |
K070664 |
03/09/2007 |
PROGENY IMAGING SOFTWARE, MODEL# 500-405 (6,7,8). |
PROGENY, INC. |
K043092 |
11/09/2004 |
PREVA, 76IN ARM, 66IN ARM, 56IN ARM, MODELS P7017, P7016, P7015 |
PROGENY, INC. |
K041831 |
07/07/2004 |
PROGENY MPSE INTRAORAL DENTAL X-RAY SENSOR |
PROGENY, INC. |
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