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)

COOK CELECT VENA CAVA FILTER

K-Number: K061815 · 2007-04-20

Decision Date2007-04-20
Product CodeDTK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

COOK CELECT VENA CAVA FILTER is the device name listed in this FDA 510(k) record. The listed applicant is William Cook Europe Aps. It received FDA 510(k) clearance on 2007-04-20 under 510(k) number K061815. The device is classified under product code DTK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COOK CELECT VENA CAVA FILTER?

COOK CELECT VENA CAVA FILTER is a medical device that received FDA 510(k) clearance on 2007-04-20. The listed applicant is William Cook Europe Aps. The 510(k) number is K061815.

When did COOK CELECT VENA CAVA FILTER receive FDA 510(k) clearance?

COOK CELECT VENA CAVA FILTER received FDA 510(k) clearance on 2007-04-20, under 510(k) number K061815.

Who is the listed applicant for COOK CELECT VENA CAVA FILTER?

The FDA 510(k) record lists William Cook Europe Aps as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COOK CELECT VENA CAVA FILTER?

The FDA product code for COOK CELECT VENA CAVA FILTER is DTK.

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 William Cook Europe Aps 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.

View all 18 devices →

Related Devices (Code: DTK)

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.

↑