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FDA 510(k)

MEDIPORT 2000 MOBILE

K-Number: K013585 · 2002-01-28

ApplicantServox Medizintechnik GmbH
Decision Date2002-01-28
Product CodeBTA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MEDIPORT 2000 MOBILE is the device name listed in this FDA 510(k) record. The listed applicant is Servox Medizintechnik GmbH. It received FDA 510(k) clearance on 2002-01-28 under 510(k) number K013585. The device is classified under product code BTA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDIPORT 2000 MOBILE?

MEDIPORT 2000 MOBILE is a medical device that received FDA 510(k) clearance on 2002-01-28. The listed applicant is Servox Medizintechnik GmbH. The 510(k) number is K013585.

When did MEDIPORT 2000 MOBILE receive FDA 510(k) clearance?

MEDIPORT 2000 MOBILE received FDA 510(k) clearance on 2002-01-28, under 510(k) number K013585.

Who is the listed applicant for MEDIPORT 2000 MOBILE?

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

What is the FDA product code for MEDIPORT 2000 MOBILE?

The FDA product code for MEDIPORT 2000 MOBILE is BTA.

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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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