COSTORSOL
K-Number: K073693 · 2008-07-03
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Device Summary
Frequently Asked Questions
What is the COSTORSOL?
COSTORSOL is a medical device that received FDA 510(k) clearance on 2008-07-03. The listed applicant is Preservation Solutions, Inc.. The 510(k) number is K073693.
When did COSTORSOL receive FDA 510(k) clearance?
COSTORSOL received FDA 510(k) clearance on 2008-07-03, under 510(k) number K073693.
Who is the listed applicant for COSTORSOL?
The FDA 510(k) record lists Preservation Solutions, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for COSTORSOL?
The FDA product code for COSTORSOL is KDN.
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 Preservation Solutions, 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: KDN)
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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