Somnus Medical Technologies, Inc.
FDA 510(k) medical device clearances.
Top product codes for Somnus Medical Technologies, Inc.
Recent clearances by Somnus Medical Technologies, Inc.
- K000720 — SOMNUS DISPOSABLE TISSUE COAGULATING ELECTRODE AND SOMNUS REUSABLE CONNECTOR CABLE
- K001438 — SOMNUS MODEL S2 ELECTROSURGICAL GENERATOR
- K000501 — ELECTROSURGICAL GENERATOR, MODEL S1
- K982717 — SOMNOPLASTY SYSTEM, MODELS S2, 1010/2010,2000/1000,1100,3000/30XX/6000, 1200
- K973701 — SOMNUS TISSUE COAGULATING ELECTRODE
- K970837 — SOMNUS MODEL 6000 DISPOSABLE TISSUE COAGULATING ELECTRODE
- K970838 — SOMNUS MODEL 30XX DISPOSABLE TRI-NEEDLE COAGULATING ELECTRODE
- K973618 — SOMNOPLASTY SYSTEM
- K971450 — SOMNOPLASTY SYSTEM
- K971711 — SOMNUS MODEL 215 ELECTROSURGICAL GENERATOR
- K970809 — BENDABLE TISSUE COAGULATING ELECTRODE WITH BENDING TOOL
- K970576 — SOMNUS MODEL 615 ELECTROSURGICAL GENERATOR(MODEL 615)
- K963884 — SOMNUS DISPOSABLE MULTIPLE ELECTRODE COAGULATING PROBE MODEL 350
- K963772 — SOMNUS MODEL 225 ELECTRO SURGICAL GENERATOR (MODEL 225)
- K961133 — SOMNUS MEDICAL TECH. MALLEABLE COAGULATING ELECTRODE
- K961132 — SOMNUS MEDICAL TECH SOFT TISSUE COAGULATING ELECTRODE
Data sourced from openFDA. This site is unofficial and independent of the FDA.