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FDA 510(k)

MMC AMPLIFIER

K-Number: K943673 · 1994-10-26

ApplicantMelville Software , Ltd.
Decision Date1994-10-26
Product CodeGWL
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MMC AMPLIFIER is the device name listed in this FDA 510(k) record. The listed applicant is Melville Software , Ltd.. It received FDA 510(k) clearance on 1994-10-26 under 510(k) number K943673. The device is classified under product code GWL. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MMC AMPLIFIER?

MMC AMPLIFIER is a medical device that received FDA 510(k) clearance on 1994-10-26. The listed applicant is Melville Software , Ltd.. The 510(k) number is K943673.

When did MMC AMPLIFIER receive FDA 510(k) clearance?

MMC AMPLIFIER received FDA 510(k) clearance on 1994-10-26, under 510(k) number K943673.

Who is the listed applicant for MMC AMPLIFIER?

The FDA 510(k) record lists Melville Software , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MMC AMPLIFIER?

The FDA product code for MMC AMPLIFIER is GWL.

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 Melville Software , Ltd. 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.

K934599SANDMAN

Related Devices (Code: GWL)

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.

K243746Delphi AmplifierQuantalx NeroscienceK242832NExT Station; NExT Station AdvancedEb Neuro S.P.A.K240646DreamClearSomnomed Technologies Inc., Doing Business AS RemwareK242305BE Plus PRO, Neurotravel LIGHTEb Neuro S.P.A.K232210X-trodes System MX-TrodesK230148VlabDormotech Medical, Ltd.

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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