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FDA 510(k)

CNS-9300 SERIES CENTRAL STATION

K-Number: K001433 · 2000-11-07

ApplicantNihon Kohden America, Inc.
Decision Date2000-11-07
Product CodeMHX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CNS-9300 SERIES CENTRAL STATION is the device name listed in this FDA 510(k) record. The listed applicant is Nihon Kohden America, Inc.. It received FDA 510(k) clearance on 2000-11-07 under 510(k) number K001433. The device is classified under product code MHX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CNS-9300 SERIES CENTRAL STATION?

CNS-9300 SERIES CENTRAL STATION is a medical device that received FDA 510(k) clearance on 2000-11-07. The listed applicant is Nihon Kohden America, Inc.. The 510(k) number is K001433.

When did CNS-9300 SERIES CENTRAL STATION receive FDA 510(k) clearance?

CNS-9300 SERIES CENTRAL STATION received FDA 510(k) clearance on 2000-11-07, under 510(k) number K001433.

Who is the listed applicant for CNS-9300 SERIES CENTRAL STATION?

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

What is the FDA product code for CNS-9300 SERIES CENTRAL STATION?

The FDA product code for CNS-9300 SERIES CENTRAL STATION is MHX.

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Other records listing Nihon Kohden America, 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.

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Related Devices (Code: MHX)

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

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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