Argon Medical Corp.
FDA 510(k) & PMA Approved Devices — 27 products
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Total Devices27
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K904994 | CLOSED SYSTEM FLUSH SET | DXT | 1991-01-15 | View |
| 510(k) | K895511 | CATHETER BALLOON DILATOR PRESSURE GAUGE | MAV | 1990-02-28 | View |
| 510(k) | K894157 | OBTURATOR | DYB | 1989-09-28 | View |
| 510(k) | K891022 | INTRODUCER FOR PTCA GUIDING CATHETERS | DYB | 1989-05-19 | View |
| 510(k) | K884375 | TRANSLUMBAR AORTOGRAPHY NEEDLE CATHETER | DQR | 1989-01-11 | View |
| 510(k) | K882221 | OVER THE NEEDLE CATHETER, ARTERIAL CATHETER NEEDLE | DYB | 1988-08-12 | View |
| 510(k) | K871297 | KADIR HI-TORQUE GUIDE WIRE | KOD | 1987-04-10 | View |
| 510(k) | K853312 | ARGON CUT BIOPSY NEEDLES, VARIOUS SIZES | DWO | 1985-09-12 | View |
| 510(k) | K852880 | PEEL-AWAY SHEATH(A COMPONENT OF ARGON INTROD SET) | DYB | 1985-08-29 | View |
| 510(k) | K844555 | PATHFINDER CARDIOVASCULAR CATHETER | DQO | 1985-03-27 | View |
| 510(k) | K842039 | ARGON DUAL LUMEN HEMODIALYSIS, CATHETER | KNZ | 1985-01-29 | View |
| 510(k) | K841926 | HYDROGLIDE SPRING GUIDE WIRES | DQX | 1985-01-02 | View |
| 510(k) | K833303 | DUOFLO 6F | DQY | 1983-12-27 | View |
| 510(k) | K832030 | HEPARIN COATED STAINLESS STEEL/TEFLON | DOX | 1983-09-29 | View |
| 510(k) | K831453 | SILCATH CENTRAL CATHETER TRAY W/18 GA | JCY | 1983-07-28 | View |
| 510(k) | K831451 | SILCATH CENTRAL CATHETER TRAY SIZE- | JCY | 1983-06-08 | View |
| 510(k) | K831171 | DIGICATH | DQO | 1983-05-25 | View |
| 510(k) | K820883 | SEPTISLEEVE | DYG | 1982-04-29 | View |
| 510(k) | K790353 | ACUTE RENAL DIALYSIS TRAY | FKG | 1979-04-20 | View |
| 510(k) | K781333 | CENTRAL CATHETER TRAY | KGC | 1978-10-24 | View |
No matching devices.
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