HEMOSIL PROS
K-Number: K053499 · 2006-01-13
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Device Summary
Frequently Asked Questions
What is the HEMOSIL PROS?
HEMOSIL PROS is a medical device that received FDA 510(k) clearance on 2006-01-13. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K053499.
When did HEMOSIL PROS receive FDA 510(k) clearance?
HEMOSIL PROS received FDA 510(k) clearance on 2006-01-13, under 510(k) number K053499.
Who is the listed applicant for HEMOSIL PROS?
The FDA 510(k) record lists Instrumentation Laboratory CO as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HEMOSIL PROS?
The FDA product code for HEMOSIL PROS is GGP.
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 Instrumentation Laboratory CO 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: GGP)
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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