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FDA 510(k)

IMLOGIX 1000 IMAGE DISPLAY SYSTEM

K-Number: K893521 · 1989-06-23

ApplicantImlogix A Div. of Microterm
Decision Date1989-06-23
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

IMLOGIX 1000 IMAGE DISPLAY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Imlogix A Div. of Microterm. It received FDA 510(k) clearance on 1989-06-23 under 510(k) number K893521. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMLOGIX 1000 IMAGE DISPLAY SYSTEM?

IMLOGIX 1000 IMAGE DISPLAY SYSTEM is a medical device that received FDA 510(k) clearance on 1989-06-23. The listed applicant is Imlogix A Div. of Microterm. The 510(k) number is K893521.

When did IMLOGIX 1000 IMAGE DISPLAY SYSTEM receive FDA 510(k) clearance?

IMLOGIX 1000 IMAGE DISPLAY SYSTEM received FDA 510(k) clearance on 1989-06-23, under 510(k) number K893521.

Who is the listed applicant for IMLOGIX 1000 IMAGE DISPLAY SYSTEM?

The FDA 510(k) record lists Imlogix A Div. of Microterm as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IMLOGIX 1000 IMAGE DISPLAY SYSTEM?

The FDA product code for IMLOGIX 1000 IMAGE DISPLAY SYSTEM is LLZ.

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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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