Peak Surgical, Inc.
FDA 510(k) & PMA Approved Devices — 7 products
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Total Devices7
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K103775 | PEAK SUCTION COAGULATOR | GEI | 2011-05-27 | View |
| 510(k) | K102709 | PEAK PLASMABLADE PLUS TISSUE DISSECTION DEVICE | GEI | 2010-12-17 | View |
| 510(k) | K102029 | PEAK PULSAR II GENERATOR MODEL PS100-102 | GEI | 2010-12-16 | View |
| 510(k) | K093695 | PEAK PLASMABLADE 3.OS TISSUE DISSECTION DEVICE | GEI | 2010-04-13 | View |
| 510(k) | K083415 | PEAK PLASMABLADE TNA TONSIL AND ADENOID TISSUE DISSECTION DEVICE | GEI | 2009-06-05 | View |
| 510(k) | K082786 | PULSAR GENERATOR, PEAK PLASMABLADE; 4.0, NEEDLE, AND EXT TISSUE DISSECTION DEVICES | GEI | 2008-12-03 | View |
| 510(k) | K073057 | PULSAR GENERATOR, MODEL PS100-100, AND PEAK PLASMABLADE TISSUE DISSECTION DEVICE, MODEL PS200-040 | GEI | 2008-07-22 | View |
No matching devices.
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