Peak Surgical, Inc.
Peak Surgical, Inc. holds FDA 510(k) medical device clearances, first cleared 2008, most recent 2011.
Top product codes for Peak Surgical, Inc.
Recent clearances by Peak Surgical, Inc.
- K103775 — PEAK SUCTION COAGULATOR
- K102709 — PEAK PLASMABLADE PLUS TISSUE DISSECTION DEVICE
- K102029 — PEAK PULSAR II GENERATOR MODEL PS100-102
- K093695 — PEAK PLASMABLADE 3.OS TISSUE DISSECTION DEVICE
- K083415 — PEAK PLASMABLADE TNA TONSIL AND ADENOID TISSUE DISSECTION DEVICE
- K082786 — PULSAR GENERATOR, PEAK PLASMABLADE; 4.0, NEEDLE, AND EXT TISSUE DISSECTION DEVICES
- K073057 — PULSAR GENERATOR, MODEL PS100-100, AND PEAK PLASMABLADE TISSUE DISSECTION DEVICE, MODEL PS200-040
Data sourced from openFDA. This site is unofficial and independent of the FDA.