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FDA 510(k)

SERIES 50XM

K-Number: K954351 · 1996-03-08

ApplicantHewlett-Packard GmbH
Decision Date1996-03-08
Product CodeHGM
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SERIES 50XM is the device name listed in this FDA 510(k) record. The listed applicant is Hewlett-Packard GmbH. It received FDA 510(k) clearance on 1996-03-08 under 510(k) number K954351. The device is classified under product code HGM. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SERIES 50XM?

SERIES 50XM is a medical device that received FDA 510(k) clearance on 1996-03-08. The listed applicant is Hewlett-Packard GmbH. The 510(k) number is K954351.

When did SERIES 50XM receive FDA 510(k) clearance?

SERIES 50XM received FDA 510(k) clearance on 1996-03-08, under 510(k) number K954351.

Who is the listed applicant for SERIES 50XM?

The FDA 510(k) record lists Hewlett-Packard GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SERIES 50XM?

The FDA product code for SERIES 50XM is HGM.

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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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