Peak Surgical, Inc.
FDA 510(k) medical device clearances.
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.