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FDA 510(k)

MIRADA RT

K-Number: K102687 · 2010-10-04

ApplicantMirada Medical, Ltd.
Decision Date2010-10-04
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MIRADA RT is the device name listed in this FDA 510(k) record. The listed applicant is Mirada Medical, Ltd.. It received FDA 510(k) clearance on 2010-10-04 under 510(k) number K102687. 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 MIRADA RT?

MIRADA RT is a medical device that received FDA 510(k) clearance on 2010-10-04. The listed applicant is Mirada Medical, Ltd.. The 510(k) number is K102687.

When did MIRADA RT receive FDA 510(k) clearance?

MIRADA RT received FDA 510(k) clearance on 2010-10-04, under 510(k) number K102687.

Who is the listed applicant for MIRADA RT?

The FDA 510(k) record lists Mirada Medical, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MIRADA RT?

The FDA product code for MIRADA RT is LLZ.

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Other records listing Mirada Medical, Ltd. 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.

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Related Devices (Code: LLZ)

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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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