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FDA 510(k)

MINGOGRAF 7

K-Number: K841868 · 1984-10-24

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1984-10-24
Product CodeDSH
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MINGOGRAF 7 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 1984-10-24 under 510(k) number K841868. The device is classified under product code DSH. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINGOGRAF 7?

MINGOGRAF 7 is a medical device that received FDA 510(k) clearance on 1984-10-24. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K841868.

When did MINGOGRAF 7 receive FDA 510(k) clearance?

MINGOGRAF 7 received FDA 510(k) clearance on 1984-10-24, under 510(k) number K841868.

Who is the listed applicant for MINGOGRAF 7?

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 MINGOGRAF 7?

The FDA product code for MINGOGRAF 7 is DSH.

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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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