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FDA 510(k)

SIEMENS MEVATRON ME

K-Number: K852907 · 1985-09-19

ApplicantSiemens Medical Laboratories, Inc.
Decision Date1985-09-19
Product CodeLHN
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SIEMENS MEVATRON ME 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 1985-09-19 under 510(k) number K852907. The device is classified under product code LHN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIEMENS MEVATRON ME?

SIEMENS MEVATRON ME is a medical device that received FDA 510(k) clearance on 1985-09-19. The listed applicant is Siemens Medical Laboratories, Inc.. The 510(k) number is K852907.

When did SIEMENS MEVATRON ME receive FDA 510(k) clearance?

SIEMENS MEVATRON ME received FDA 510(k) clearance on 1985-09-19, under 510(k) number K852907.

Who is the listed applicant for SIEMENS MEVATRON ME?

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 SIEMENS MEVATRON ME?

The FDA product code for SIEMENS MEVATRON ME is LHN.

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Other records listing Siemens Medical Laboratories, Inc. as applicant

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Related Devices (Code: LHN)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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