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FDA 510(k)

MIRAGE CEDARS OPTION

K-Number: K070683 · 2007-04-12

ApplicantSegami Corporation
Decision Date2007-04-12
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MIRAGE CEDARS OPTION is the device name listed in this FDA 510(k) record. The listed applicant is Segami Corporation. It received FDA 510(k) clearance on 2007-04-12 under 510(k) number K070683. 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 MIRAGE CEDARS OPTION?

MIRAGE CEDARS OPTION is a medical device that received FDA 510(k) clearance on 2007-04-12. The listed applicant is Segami Corporation. The 510(k) number is K070683.

When did MIRAGE CEDARS OPTION receive FDA 510(k) clearance?

MIRAGE CEDARS OPTION received FDA 510(k) clearance on 2007-04-12, under 510(k) number K070683.

Who is the listed applicant for MIRAGE CEDARS OPTION?

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

What is the FDA product code for MIRAGE CEDARS OPTION?

The FDA product code for MIRAGE CEDARS OPTION is LLZ.

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Other records listing Segami Corporation 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.

K071584OASIS RELEASE 1.0K070397DGSCOPE, RELEASE 1.0K043441MIRAGE, RELEASE 5.5

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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