FDA 510(k) Applications Submitted by FORTUNE MEDICAL INSTRUMENT CORP.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K014002 |
12/04/2001 |
ALL SILICONE SUPRA-PUBIA CATHETER, MODELS 4880/4890 |
FORTUNE MEDICAL INSTRUMENT CORP. |
| K022112 |
06/28/2002 |
FORTUNE ALL SILICONE STOMACH (GASTRIC) TUBES, MODEL 2020 |
FORTUNE MEDICAL INSTRUMENT CORP. |
| K980917 |
03/11/1998 |
ALL SLICONE DRAINAGE, PENROSE DRAIN, CWV DRAIN, THORACIC DRAIN TUBES AND CWV RESERVOIR |
FORTUNE MEDICAL INSTRUMENT CORP. |
| K980919 |
03/11/1998 |
ALL SILICONE 2-WAY & 3-WAY FOLY BALLOON CATHETER AND NELATON CATHETER |
FORTUNE MEDICAL INSTRUMENT CORP. |
| K021193 |
04/15/2002 |
FORTUNE SILICONE VACUUM SUCTION, MODEL #1300 |
FORTUNE MEDICAL INSTRUMENT CORP. |
| K021142 |
04/09/2002 |
ALL SILICONE HEMATURIA CATHETER, MODELS 4861, 4862, 4863, 4864, 4865 |
FORTUNE MEDICAL INSTRUMENT CORP. |
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