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FDA 510(k)

MIM 4.1 (SEASTAR)

K-Number: K071964 · 2007-09-26

ApplicantMimvista Corp.
Decision Date2007-09-26
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MIM 4.1 (SEASTAR) is the device name listed in this FDA 510(k) record. The listed applicant is Mimvista Corp.. It received FDA 510(k) clearance on 2007-09-26 under 510(k) number K071964. 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 MIM 4.1 (SEASTAR)?

MIM 4.1 (SEASTAR) is a medical device that received FDA 510(k) clearance on 2007-09-26. The listed applicant is Mimvista Corp.. The 510(k) number is K071964.

When did MIM 4.1 (SEASTAR) receive FDA 510(k) clearance?

MIM 4.1 (SEASTAR) received FDA 510(k) clearance on 2007-09-26, under 510(k) number K071964.

Who is the listed applicant for MIM 4.1 (SEASTAR)?

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

What is the FDA product code for MIM 4.1 (SEASTAR)?

The FDA product code for MIM 4.1 (SEASTAR) is LLZ.

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 Mimvista Corp. 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.

K062163MIMVIEWERK060816MIM 4.0 (NEUROK052379MIM 3.5 (CIRCA)

Related Devices (Code: LLZ)

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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