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FDA 510(k)

LIFE SCOPE P, MODEL BSM-4100 SERIES

K-Number: K001693 · 2000-10-24

ApplicantNihon Kohden America, Inc.
Decision Date2000-10-24
Product CodeMHX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LIFE SCOPE P, MODEL BSM-4100 SERIES 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 2000-10-24 under 510(k) number K001693. 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 LIFE SCOPE P, MODEL BSM-4100 SERIES?

LIFE SCOPE P, MODEL BSM-4100 SERIES is a medical device that received FDA 510(k) clearance on 2000-10-24. The listed applicant is Nihon Kohden America, Inc.. The 510(k) number is K001693.

When did LIFE SCOPE P, MODEL BSM-4100 SERIES receive FDA 510(k) clearance?

LIFE SCOPE P, MODEL BSM-4100 SERIES received FDA 510(k) clearance on 2000-10-24, under 510(k) number K001693.

Who is the listed applicant for LIFE SCOPE P, MODEL BSM-4100 SERIES?

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 LIFE SCOPE P, MODEL BSM-4100 SERIES?

The FDA product code for LIFE SCOPE P, MODEL BSM-4100 SERIES is MHX.

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Other records listing Nihon Kohden America, Inc. as applicant

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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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