ACUEITY MEDICAL LIGHT SOURCE
K-Number: K032430 · 2003-09-05
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Device Summary
Frequently Asked Questions
What is the ACUEITY MEDICAL LIGHT SOURCE?
ACUEITY MEDICAL LIGHT SOURCE is a medical device that received FDA 510(k) clearance on 2003-09-05. The listed applicant is Acueity, Inc.. The 510(k) number is K032430.
When did ACUEITY MEDICAL LIGHT SOURCE receive FDA 510(k) clearance?
ACUEITY MEDICAL LIGHT SOURCE received FDA 510(k) clearance on 2003-09-05, under 510(k) number K032430.
Who is the listed applicant for ACUEITY MEDICAL LIGHT SOURCE?
The FDA 510(k) record lists Acueity, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ACUEITY MEDICAL LIGHT SOURCE?
The FDA product code for ACUEITY MEDICAL LIGHT SOURCE is FCW.
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 Acueity, 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: FCW)
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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