FDA 510(k)

MIP MR

K-Number: K891692 · 1989-10-27

Decision Date1989-10-27

Product CodeLLZ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

MIP MR is the device name listed in this FDA 510(k) record. The listed applicant is Kontron Electronics. It received FDA 510(k) clearance on 1989-10-27 under 510(k) number K891692. 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 MIP MR?

MIP MR is a medical device that received FDA 510(k) clearance on 1989-10-27. The listed applicant is Kontron Electronics. The 510(k) number is K891692.

When did MIP MR receive FDA 510(k) clearance?

MIP MR received FDA 510(k) clearance on 1989-10-27, under 510(k) number K891692.

Who is the listed applicant for MIP MR?

The FDA 510(k) record lists Kontron Electronics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MIP MR?

The FDA product code for MIP MR is LLZ.

Other records listing Kontron Electronics 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.

K891689MIPRON/UMIPRON K892712MIP/CT IMAGE PROCESSING WORKSTATION

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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.