FDA 510(k)

SOMNUS MODEL 6000 DISPOSABLE TISSUE COAGULATING ELECTRODE

K-Number: K970837 · 1998-01-09

ApplicantSomnus Medical Technologies, Inc.

Decision Date1998-01-09

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

SOMNUS MODEL 6000 DISPOSABLE TISSUE COAGULATING ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Somnus Medical Technologies, Inc.. It received FDA 510(k) clearance on 1998-01-09 under 510(k) number K970837. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SOMNUS MODEL 6000 DISPOSABLE TISSUE COAGULATING ELECTRODE?

SOMNUS MODEL 6000 DISPOSABLE TISSUE COAGULATING ELECTRODE is a medical device that received FDA 510(k) clearance on 1998-01-09. The listed applicant is Somnus Medical Technologies, Inc.. The 510(k) number is K970837.

When did SOMNUS MODEL 6000 DISPOSABLE TISSUE COAGULATING ELECTRODE receive FDA 510(k) clearance?

SOMNUS MODEL 6000 DISPOSABLE TISSUE COAGULATING ELECTRODE received FDA 510(k) clearance on 1998-01-09, under 510(k) number K970837.

Who is the listed applicant for SOMNUS MODEL 6000 DISPOSABLE TISSUE COAGULATING ELECTRODE?

The FDA 510(k) record lists Somnus Medical Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SOMNUS MODEL 6000 DISPOSABLE TISSUE COAGULATING ELECTRODE?

The FDA product code for SOMNUS MODEL 6000 DISPOSABLE TISSUE COAGULATING ELECTRODE is GEI.

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Other records listing Somnus Medical Technologies, Inc. as applicant

K000720SOMNUS DISPOSABLE TISSUE COAGULATING ELECTRODE AND SOMNUS REUSABLE CONNECTOR CABLE K001438SOMNUS MODEL S2 ELECTROSURGICAL GENERATOR K000501ELECTROSURGICAL GENERATOR, MODEL S1 K982717SOMNOPLASTY SYSTEM, MODELS S2, 1010/2010,2000/1000,1100,3000/30XX/6000, 1200 K973701SOMNUS TISSUE COAGULATING ELECTRODE K970838SOMNUS MODEL 30XX DISPOSABLE TRI-NEEDLE COAGULATING ELECTRODE

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.