AOS ORION IR-192 SOURCE CABLE
K-Number: K102811 · 2011-06-02
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Device Summary
Frequently Asked Questions
What is the AOS ORION IR-192 SOURCE CABLE?
AOS ORION IR-192 SOURCE CABLE is a medical device that received FDA 510(k) clearance on 2011-06-02. The listed applicant is Alpha-Omega Services, Inc.. The 510(k) number is K102811.
When did AOS ORION IR-192 SOURCE CABLE receive FDA 510(k) clearance?
AOS ORION IR-192 SOURCE CABLE received FDA 510(k) clearance on 2011-06-02, under 510(k) number K102811.
Who is the listed applicant for AOS ORION IR-192 SOURCE CABLE?
The FDA 510(k) record lists Alpha-Omega Services, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AOS ORION IR-192 SOURCE CABLE?
The FDA product code for AOS ORION IR-192 SOURCE CABLE is KXK.
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 Alpha-Omega Services, 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: KXK)
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.
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