Pajunk GmbH
FDA 510(k) & PMA Approved Devices — 19 products
Advertisement
Total Devices19
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K113207 | SONO TAP, TUOHY SONO | BSP | 2012-02-29 | View |
| 510(k) | K113209 | CHIBA SONO | KNW | 2011-11-21 | View |
| 510(k) | K060563 | EPISPIN, EPISPIN II SAFETY, EPISPIN II, EPISPIN I, EPISPIN IV | CAZ | 2006-06-02 | View |
| 510(k) | K053283 | UNIPLEX NANOLINE CANNULA, PLEXOLONG NANOLINE SET, STIMULONG NANOLINE SET | CAZ | 2006-01-12 | View |
| 510(k) | K053282 | ADAPTABLE MONOPOLAR ELECTRODES WITH CERAMIC TIP | GEI | 2005-12-13 | View |
| 510(k) | K043130 | MODIFICATION TO PAJUNK STIMULONG PLUS CATHETER SETS | CAZ | 2004-12-21 | View |
| 510(k) | K042979 | MODIFICATION TO: PLEXALONG SETS | BSP | 2004-12-21 | View |
| 510(k) | K040965 | PAJUNK TUOHY NEEDLES, QUINCKE NEEDLES, CHIBA NEEDLES & CRAWFORD NEEDLES | BSP | 2004-09-07 | View |
| 510(k) | K033018 | STIMULONG PLUS CATHETER SET MODEL, VARIOUS | CAZ | 2004-05-05 | View |
| 510(k) | K033249 | PAJUNK MODULAR HANDLE INSTRUMENTS | GCJ | 2004-03-05 | View |
| 510(k) | K023218 | MODIFICATION TO PLEXOLONG SETS | BSP | 2003-03-24 | View |
| 510(k) | K013041 | PLEXOLONG SETS | CAZ | 2002-06-11 | View |
| 510(k) | K011308 | MULTISTIM | BXN | 2001-11-29 | View |
| 510(k) | K012771 | TROCAR SLEEVE AND ACCESSORIES, MODELS 1287-XX-XX | GCJ | 2001-11-14 | View |
| 510(k) | K011997 | MODULAR VALVE HANDLES FOR ADAPTABLE TUBES, MODEL 1298-XX-XX, 1295-XX-XX | GCJ | 2001-07-10 | View |
| 510(k) | K000722 | UNIPOLAR NEEDLES | BSP | 2000-03-31 | View |
| 510(k) | K911221 | ATRAUMATIC SPECIAL SPROTTE NEEDLE | BSP | 1992-07-24 | View |
| 510(k) | K911202 | ATRAUMATIC STANDARD SPROTTE NEEDLE | BSP | 1992-05-04 | View |
| 510(k) | K911260 | ATRAUMATIC STANDARD SPROTTE NEEDLE | BSP | 1991-10-21 | View |
No matching devices.
Advertisement