Peak Surgical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PEAK SUCTION COAGULATOR, PEAK PLASMABLADE PLUS TISSUE DISSECTION DEVICE, PEAK PULSAR II GENERATOR MODEL PS100-102
7
Total
7
Cleared
0
Denied
FDA 510(k) Regulatory Record - Peak Surgical, Inc. General & Plastic Surgery ✕
7 devices
Cleared
May 27, 2011
PEAK SUCTION COAGULATOR
General & Plastic Surgery
151d
Cleared
Dec 17, 2010
PEAK PLASMABLADE PLUS TISSUE DISSECTION DEVICE
General & Plastic Surgery
88d
Cleared
Dec 16, 2010
PEAK PULSAR II GENERATOR MODEL PS100-102
General & Plastic Surgery
150d
Cleared
Apr 13, 2010
PEAK PLASMABLADE 3.OS TISSUE DISSECTION DEVICE
General & Plastic Surgery
134d
Cleared
Jun 05, 2009
PEAK PLASMABLADE TNA TONSIL AND ADENOID TISSUE DISSECTION DEVICE
General & Plastic Surgery
199d
Cleared
Dec 03, 2008
PULSAR GENERATOR, PEAK PLASMABLADE
General & Plastic Surgery
71d
Cleared
Jul 22, 2008
PULSAR GENERATOR, MODEL PS100-100, AND PEAK PLASMABLADE TISSUE DISSECTION...
General & Plastic Surgery
266d