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FDA 510(k)

MEVASSIST(SETUP CONTROLLER)

K-Number: K852609 · 1986-02-06

ApplicantMagus Microcontrollers, Inc.
Decision Date1986-02-06
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MEVASSIST(SETUP CONTROLLER) 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 1986-02-06 under 510(k) number K852609. 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 MEVASSIST(SETUP CONTROLLER)?

MEVASSIST(SETUP CONTROLLER) is a medical device that received FDA 510(k) clearance on 1986-02-06. The listed applicant is Magus Microcontrollers, Inc.. The 510(k) number is K852609.

When did MEVASSIST(SETUP CONTROLLER) receive FDA 510(k) clearance?

MEVASSIST(SETUP CONTROLLER) received FDA 510(k) clearance on 1986-02-06, under 510(k) number K852609.

Who is the listed applicant for MEVASSIST(SETUP CONTROLLER)?

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 MEVASSIST(SETUP CONTROLLER)?

The FDA product code for MEVASSIST(SETUP CONTROLLER) 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.

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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.

K864910MEVACHECK

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.

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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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