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FDA 510(k)

MEVACHECK

K-Number: K864910 · 1987-03-16

Decision Date1987-03-16
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MEVACHECK is the device name listed in this FDA 510(k) record. The listed applicant is Magus Microcontrollers, Inc.. It received FDA 510(k) clearance on 1987-03-16 under 510(k) number K864910. 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 MEVACHECK?

MEVACHECK is a medical device that received FDA 510(k) clearance on 1987-03-16. The listed applicant is Magus Microcontrollers, Inc.. The 510(k) number is K864910.

When did MEVACHECK receive FDA 510(k) clearance?

MEVACHECK received FDA 510(k) clearance on 1987-03-16, under 510(k) number K864910.

Who is the listed applicant for MEVACHECK?

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

What is the FDA product code for MEVACHECK?

The FDA product code for MEVACHECK is IYE.

Related Clinical Trials

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.

Other records listing Magus Microcontrollers, Inc. as applicant

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.

Related Devices (Code: IYE)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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