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FDA 510(k)

MINGOGRAF 410

K-Number: K864009 · 1987-01-12

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1987-01-12
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MINGOGRAF 410 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 1987-01-12 under 510(k) number K864009. The device is classified under product code DPS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINGOGRAF 410?

MINGOGRAF 410 is a medical device that received FDA 510(k) clearance on 1987-01-12. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K864009.

When did MINGOGRAF 410 receive FDA 510(k) clearance?

MINGOGRAF 410 received FDA 510(k) clearance on 1987-01-12, under 510(k) number K864009.

Who is the listed applicant for MINGOGRAF 410?

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 410?

The FDA product code for MINGOGRAF 410 is DPS.

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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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