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FDA 510(k)

MSI S-500L RF GENERATOR

K-Number: K041980 · 2004-08-06

ApplicantMedsphere International, Inc.
Decision Date2004-08-06
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MSI S-500L RF GENERATOR is the device name listed in this FDA 510(k) record. The listed applicant is Medsphere International, Inc.. It received FDA 510(k) clearance on 2004-08-06 under 510(k) number K041980. 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 MSI S-500L RF GENERATOR?

MSI S-500L RF GENERATOR is a medical device that received FDA 510(k) clearance on 2004-08-06. The listed applicant is Medsphere International, Inc.. The 510(k) number is K041980.

When did MSI S-500L RF GENERATOR receive FDA 510(k) clearance?

MSI S-500L RF GENERATOR received FDA 510(k) clearance on 2004-08-06, under 510(k) number K041980.

Who is the listed applicant for MSI S-500L RF GENERATOR?

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

What is the FDA product code for MSI S-500L RF GENERATOR?

The FDA product code for MSI S-500L RF 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.

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Other records listing Medsphere International, 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.

K033888MSI MODEL S-500 RF GENERATORK030996MSI SA ELECTRODESK024266MSI TA ELECTRODES

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.

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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.

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