SOMNUS MODEL 215 ELECTROSURGICAL GENERATOR
K-Number: K971711 · 1997-06-24
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Device Summary
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.
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.
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