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FDA 510(k)

MEISINGER BENEX, MODEL BE001

K-Number: K062130 · 2007-04-16

ApplicantHager& Meisinger GmbH
Decision Date2007-04-16
Product CodeEMG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MEISINGER BENEX, MODEL BE001 is the device name listed in this FDA 510(k) record. The listed applicant is Hager& Meisinger GmbH. It received FDA 510(k) clearance on 2007-04-16 under 510(k) number K062130. The device is classified under product code EMG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEISINGER BENEX, MODEL BE001?

MEISINGER BENEX, MODEL BE001 is a medical device that received FDA 510(k) clearance on 2007-04-16. The listed applicant is Hager& Meisinger GmbH. The 510(k) number is K062130.

When did MEISINGER BENEX, MODEL BE001 receive FDA 510(k) clearance?

MEISINGER BENEX, MODEL BE001 received FDA 510(k) clearance on 2007-04-16, under 510(k) number K062130.

Who is the listed applicant for MEISINGER BENEX, MODEL BE001?

The FDA 510(k) record lists Hager& Meisinger GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEISINGER BENEX, MODEL BE001?

The FDA product code for MEISINGER BENEX, MODEL BE001 is EMG.

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Related Devices (Code: EMG)

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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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