FDA 510(k) Applications Submitted by TELEMED SYSTEMS, INC.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K992390 |
07/19/1999 |
HOT BIOPSY FORCEPS FEENESTRATED 230 CM OVAL CUP, HOT BIOPSY FORCEPS SERRATED 160 CM OVAL CUP, HOT BIOPSY FORCEPS SERRATD |
TELEMED SYSTEMS, INC. |
K992402 |
07/19/1999 |
5.0 FRENCH X 200CM X 35MM TIP TAPER-20MM CUTTING WIRE, 5.0 FRENCH X 200CM X 35MM TIP TAPER-30MM CUTTING WIRE, 5.0 FRENCH |
TELEMED SYSTEMS, INC. |
K020379 |
02/05/2002 |
PPD BALLOON DILATATION CATHETER |
TELEMED SYSTEMS, INC. |
K010412 |
02/12/2001 |
FLEXIBLE ENDOSCOPIC SCISSORS |
TELEMED SYSTEMS, INC. |
K013737 |
11/13/2001 |
MODIFICATION TO: 3-LUMEN DURALON OCCLUSION BALLOON |
TELEMED SYSTEMS, INC. |
K974300 |
11/17/1997 |
TELEMED SYSTEMS RETRIEVAL BASKET |
TELEMED SYSTEMS, INC. |
K974312 |
11/17/1997 |
REUSABLE BIOPSY FORCEPS OVAL CUP, REUSABLE BIOSY FORCEPS OVAL CUP W/NEEDLE, REUSABLE BIOPSY FORCEPS SERRATED CUP, REUSAR |
TELEMED SYSTEMS, INC. |
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