EAGLE - NEODYUMIUM DOPED YTTRIUM ALUMINUM GARNET
K-Number: K885257 · 1989-06-05
Advertisement
Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement