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FDA 510(k)

MODIFICATION TO MIRAGE

K-Number: K010726 · 2001-04-26

ApplicantSegami Corp., Inc.
Decision Date2001-04-26
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO MIRAGE is the device name listed in this FDA 510(k) record. The listed applicant is Segami Corp., Inc.. It received FDA 510(k) clearance on 2001-04-26 under 510(k) number K010726. 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 MODIFICATION TO MIRAGE?

MODIFICATION TO MIRAGE is a medical device that received FDA 510(k) clearance on 2001-04-26. The listed applicant is Segami Corp., Inc.. The 510(k) number is K010726.

When did MODIFICATION TO MIRAGE receive FDA 510(k) clearance?

MODIFICATION TO MIRAGE received FDA 510(k) clearance on 2001-04-26, under 510(k) number K010726.

Who is the listed applicant for MODIFICATION TO MIRAGE?

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

What is the FDA product code for MODIFICATION TO MIRAGE?

The FDA product code for MODIFICATION TO MIRAGE is LLZ.

Related Clinical Trials

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Other records listing Segami Corp., 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.

K972886MIRAGE

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

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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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