PAROS CRP
K-Number: K022690 · 2002-12-23
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Device Summary
Frequently Asked Questions
What is the PAROS CRP?
PAROS CRP is a medical device that received FDA 510(k) clearance on 2002-12-23. The listed applicant is Horiba, Ltd.. The 510(k) number is K022690.
When did PAROS CRP receive FDA 510(k) clearance?
PAROS CRP received FDA 510(k) clearance on 2002-12-23, under 510(k) number K022690.
Who is the listed applicant for PAROS CRP?
The FDA 510(k) record lists Horiba, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PAROS CRP?
The FDA product code for PAROS CRP is DCN.
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 Horiba, Ltd. 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: DCN)
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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