Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

PAROS CRP

K-Number: K022690 · 2002-12-23

ApplicantHoriba, Ltd.
Decision Date2002-12-23
Product CodeDCN
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

PAROS CRP is the device name listed in this FDA 510(k) record. The listed applicant is Horiba, Ltd.. It received FDA 510(k) clearance on 2002-12-23 under 510(k) number K022690. The device is classified under product code DCN. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

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.

↑