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FDA 510(k)

MSI SA ELECTRODES

K-Number: K030996 · 2003-05-30

ApplicantMedsphere International, Inc.
Decision Date2003-05-30
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MSI SA ELECTRODES 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 2003-05-30 under 510(k) number K030996. 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 SA ELECTRODES?

MSI SA ELECTRODES is a medical device that received FDA 510(k) clearance on 2003-05-30. The listed applicant is Medsphere International, Inc.. The 510(k) number is K030996.

When did MSI SA ELECTRODES receive FDA 510(k) clearance?

MSI SA ELECTRODES received FDA 510(k) clearance on 2003-05-30, under 510(k) number K030996.

Who is the listed applicant for MSI SA ELECTRODES?

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 SA ELECTRODES?

The FDA product code for MSI SA ELECTRODES 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.

K041980MSI S-500L RF GENERATORK033888MSI MODEL S-500 RF GENERATORK024266MSI TA ELECTRODES

Related Devices (Code: GEI)

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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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