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FDA 510(k)

EAGLE - NEODYUMIUM DOPED YTTRIUM ALUMINUM GARNET

K-Number: K885257 · 1989-06-05

Decision Date1989-06-05
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

EAGLE - NEODYUMIUM DOPED YTTRIUM ALUMINUM GARNET is the device name listed in this FDA 510(k) record. The listed applicant is Living Technology, Inc.. It received FDA 510(k) clearance on 1989-06-05 under 510(k) number K885257. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EAGLE - NEODYUMIUM DOPED YTTRIUM ALUMINUM GARNET?

EAGLE - NEODYUMIUM DOPED YTTRIUM ALUMINUM GARNET is a medical device that received FDA 510(k) clearance on 1989-06-05. The listed applicant is Living Technology, Inc.. The 510(k) number is K885257.

When did EAGLE - NEODYUMIUM DOPED YTTRIUM ALUMINUM GARNET receive FDA 510(k) clearance?

EAGLE - NEODYUMIUM DOPED YTTRIUM ALUMINUM GARNET received FDA 510(k) clearance on 1989-06-05, under 510(k) number K885257.

Who is the listed applicant for EAGLE - NEODYUMIUM DOPED YTTRIUM ALUMINUM GARNET?

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

What is the FDA product code for EAGLE - NEODYUMIUM DOPED YTTRIUM ALUMINUM GARNET?

The FDA product code for EAGLE - NEODYUMIUM DOPED YTTRIUM ALUMINUM GARNET is GEX. This falls under the Gastroenterology category.

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.

Other records listing Living Technology, 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.

Related Devices (Code: GEX)

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.

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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