FDA 510(k)

MEVATRON 74

K-Number: K790747 · 1979-05-04

ApplicantSiemens Medical Laboratories, Inc.

Decision Date1979-05-04

Product CodeIYE

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

MEVATRON 74 is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Laboratories, Inc.. It received FDA 510(k) clearance on 1979-05-04 under 510(k) number K790747. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEVATRON 74?

MEVATRON 74 is a medical device that received FDA 510(k) clearance on 1979-05-04. The listed applicant is Siemens Medical Laboratories, Inc.. The 510(k) number is K790747.

When did MEVATRON 74 receive FDA 510(k) clearance?

MEVATRON 74 received FDA 510(k) clearance on 1979-05-04, under 510(k) number K790747.

Who is the listed applicant for MEVATRON 74?

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

What is the FDA product code for MEVATRON 74?

The FDA product code for MEVATRON 74 is IYE.

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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.