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FDA 510(k)

MEVATRON, M 2 CLASS

K-Number: K882729 · 1988-09-19

ApplicantSiemens Medical Laboratories, Inc.
Decision Date1988-09-19
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MEVATRON, M 2 CLASS 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 1988-09-19 under 510(k) number K882729. 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, M 2 CLASS?

MEVATRON, M 2 CLASS is a medical device that received FDA 510(k) clearance on 1988-09-19. The listed applicant is Siemens Medical Laboratories, Inc.. The 510(k) number is K882729.

When did MEVATRON, M 2 CLASS receive FDA 510(k) clearance?

MEVATRON, M 2 CLASS received FDA 510(k) clearance on 1988-09-19, under 510(k) number K882729.

Who is the listed applicant for MEVATRON, M 2 CLASS?

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, M 2 CLASS?

The FDA product code for MEVATRON, M 2 CLASS is IYE.

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Other records listing Siemens Medical Laboratories, Inc. as applicant

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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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