AQUARIUSAPS SERVER
K-Number: K061214 · 2006-05-15
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Device Summary
Frequently Asked Questions
What is the AQUARIUSAPS SERVER?
AQUARIUSAPS SERVER is a medical device that received FDA 510(k) clearance on 2006-05-15. The listed applicant is Terarecon,Inc.. The 510(k) number is K061214.
When did AQUARIUSAPS SERVER receive FDA 510(k) clearance?
AQUARIUSAPS SERVER received FDA 510(k) clearance on 2006-05-15, under 510(k) number K061214.
Who is the listed applicant for AQUARIUSAPS SERVER?
The FDA 510(k) record lists Terarecon,Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AQUARIUSAPS SERVER?
The FDA product code for AQUARIUSAPS SERVER is LLZ.
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 Terarecon,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: 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.
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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