Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

SOMNUS MODEL 215 ELECTROSURGICAL GENERATOR

K-Number: K971711 · 1997-06-24

Decision Date1997-06-24
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SOMNUS MODEL 215 ELECTROSURGICAL GENERATOR 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 1997-06-24 under 510(k) number K971711. 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 215 ELECTROSURGICAL GENERATOR?

SOMNUS MODEL 215 ELECTROSURGICAL GENERATOR is a medical device that received FDA 510(k) clearance on 1997-06-24. The listed applicant is Somnus Medical Technologies, Inc.. The 510(k) number is K971711.

When did SOMNUS MODEL 215 ELECTROSURGICAL GENERATOR receive FDA 510(k) clearance?

SOMNUS MODEL 215 ELECTROSURGICAL GENERATOR received FDA 510(k) clearance on 1997-06-24, under 510(k) number K971711.

Who is the listed applicant for SOMNUS MODEL 215 ELECTROSURGICAL GENERATOR?

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 215 ELECTROSURGICAL GENERATOR?

The FDA product code for SOMNUS MODEL 215 ELECTROSURGICAL GENERATOR is GEI.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Somnus Medical Technologies, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 16 devices →

Related Devices (Code: GEI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

View on FDA Database →

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

↑