FDA 510(k) Applications Submitted by TAMARA YOUNT
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K020715 |
03/05/2002 |
PHILIPS M5066A AND M5068A |
PHILIPS MEDICAL SYSTEMS |
| K970842 |
03/07/1997 |
Cordis Endeavor Infusion Catheter |
CORDIS CORP. |
| K111693 |
06/16/2011 |
PHILIPS HEARTSTART FR3 AUTOMATED EXTERNAL DEFIBRILLATOR |
PHILIPS MEDICAL SYSTEMS |
| K051632 |
06/20/2005 |
PHILIPS HEARTSTART FR2+ AUTOMATED EXTERNAL DEFIBRILLATOR, MODELS M3860A, M3861A, M3840A, M3841A |
PHILIPS MEDICAL SYSTEMS |
| K963000 |
08/02/1996 |
MAXI LD PTA BALLOON CATHETER |
CORDIS CORP. |
| K013425 |
10/16/2001 |
HEARTSTREAM/HEARTSTART FR2 AED ECG CABLE, MODELS M3860A, M3861A, M3840A, M3841A |
PHILIPS MEDICAL SYSTEMS |
| K014157 |
12/19/2001 |
HEARTSTREAMFR2 AED WITH M3848A AND M3849A, MODELS M3860A, M3861, M3840A, M3841A |
PHILIPS MEDICAL SYSTEMS |
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