Meadox Surgimed, Inc.
FDA 510(k) & PMA Approved Devices — 24 products
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Total Devices24
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K944143 | MS CLASSIQUE BALLOON CATHETER | FGE | 1995-03-13 | View |
| 510(k) | K945061 | NOPROFILE OLBERT CATHETER SYSTEM | KOD | 1995-03-09 | View |
| 510(k) | K942382 | MS AMPLATZ EXTRA STIFF GUIDE WIRE | DQX | 1994-08-22 | View |
| 510(k) | K930201 | ACECUT SUTOMATIC BIOPSY SYSTEM | KNW | 1993-06-09 | View |
| 510(k) | K911635 | MEADOX(R) SURGIMED(R) BIOPSY GUN II | KNW | 1991-06-20 | View |
| 510(k) | K905181 | NO PROFILE OLBERT CATHETER SYSTEM FOR UROLOGY | EZN | 1991-03-06 | View |
| 510(k) | K904582 | QUICKWIRE - HYDROPHILIC COATED GUIDEWIRE | DQX | 1991-02-25 | View |
| 510(k) | K904983 | MEADOX(R) SURGIMED OLBERT CATH SYST FOR UROLOGY | EZN | 1991-01-30 | View |
| 510(k) | K902461 | MEADOX SURGIMED BIOPSY GUN AND NEEDLE | KNW | 1990-07-16 | View |
| 510(k) | K890926 | SURECUT BMB BONE MARROW BIOPSY/ASPIRATION NEEDLE | FMI | 1989-06-20 | View |
| 510(k) | K863218 | CYTOSTATIC FILTRATION SET | LFK | 1987-02-12 | View |
| 510(k) | K861267 | UROCUT BIOPSY NEEDLE | KNW | 1987-01-20 | View |
| 510(k) | K862742 | NEPHROSTOMY SET | LJE | 1986-10-31 | View |
| 510(k) | K862550 | OLBERT CATHETER SYSTEM WITH SIDEWINDER CURVE | LIT | 1986-09-02 | View |
| 510(k) | K860430 | THE NAVIGATOR STEERABLE GUIDE WIRE | DQX | 1986-07-18 | View |
| 510(k) | K861220 | LUNDERQUIST - RING PTC DRAINAGE CATHETER | FGE | 1986-05-19 | View |
| 510(k) | K860429 | MEADOX SURGIMED GUIDE CATHETER | DQO | 1986-04-23 | View |
| 510(k) | K854262 | MEADOX SURGIMED BREAST LOCALIZATION WIRE SET/ONLY | FZX | 1985-12-24 | View |
| 510(k) | K854404 | ROTEX SCREW BIOPSY NEEDLE | FCG | 1985-12-02 | View |
| 510(k) | K854420 | MEADOX SURGIMED A/S THREE PIECE SCREW BIOPSY NEEDL | GDM | 1985-11-22 | View |
No matching devices.
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