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FDA 510(k)

THORAX FD AND MULTIX FD

K-Number: K983732 · 1999-04-21

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1999-04-21
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

THORAX FD AND MULTIX FD is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 1999-04-21 under 510(k) number K983732. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THORAX FD AND MULTIX FD?

THORAX FD AND MULTIX FD is a medical device that received FDA 510(k) clearance on 1999-04-21. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K983732.

When did THORAX FD AND MULTIX FD receive FDA 510(k) clearance?

THORAX FD AND MULTIX FD received FDA 510(k) clearance on 1999-04-21, under 510(k) number K983732.

Who is the listed applicant for THORAX FD AND MULTIX FD?

The FDA 510(k) record lists Siemens Medical Solutions USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THORAX FD AND MULTIX FD?

The FDA product code for THORAX FD AND MULTIX FD is MQB.

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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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