FDA 510(k) Applications Submitted by FRANK TIGHE
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K000416 |
02/08/2000 |
TRANSPAK (VITREORETINAL INFUSION PAK), MODELS 90000, 90001 |
RETINALABS.COM |
| K000418 |
02/08/2000 |
PDT DOSECALCULATOR, MODEL 80000 |
RETINALABS.COM |
| K000420 |
02/08/2000 |
SILICONE OIL EXPRESS (INFUSION PAK), MODELS 10000, 10001, 10002, 10003 |
RETINALABS.COM |
| K000457 |
02/11/2000 |
VERTEFUSION-PHOTODYNAMIC THERAPY PAK, MODEL 11000 SERIES; PHOTOFUSION-PHOTODYNAMIC THERAPY PAK, MODEL 12000 SERIES |
RETINALABS.COM |
| K003036 |
09/29/2000 |
TURBO-FLOW INFUSION CANNULA 19 GAGE,20 GAGE,23 GAGE, 25 GAGE, MODEL 101019,101020,101023,101025 |
RETINALABS.COM |
| K970873 |
03/10/1997 |
ENDOSOFT SOFT TIP NEEDLE (20 GA. AND 19 GA.) |
AMERICAN MEDICAL DEVICES, INC. |
| K970875 |
03/10/1997 |
ENDOLIGHT FIBEROPTIC ENDO-ILLUMINATOR (20 GA. & 19 GA.) |
AMERICAN MEDICAL DEVICES, INC. |
| K970878 |
03/10/1997 |
ENDOLIGHT FIBEROPTIC REGULAR MONOFILAMENT AND FINE MONOFILAMENT |
AMERICAN MEDICAL DEVICES, INC. |
| K970882 |
03/10/1997 |
ENDOLIGHT END IRRIGATING ENDO-ILLUMINATOR (20 GA. AND 19 GA.) |
AMERICAN MEDICAL DEVICES, INC. |
| K971853 |
05/20/1997 |
ENDOVIEW SPPHIRE LENS SET |
AMERICAN MEDICAL DEVICES, INC. |
| K974561 |
12/05/1997 |
MOISTAIR FLUID AIR TUBING SET |
AMERICAN MEDICAL DEVICES, INC. |
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