Somnus Medical Technologies, Inc.
Somnus Medical Technologies, Inc. holds FDA 510(k) medical device clearances, first cleared 1996, most recent 2000.
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.