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FDA 510(k)

ARTERIAL 20/40 MICRON FILTERS W/WO HEPARIN COATING

K-Number: K864262 · 1987-01-02

Decision Date1987-01-02
Product CodeDTM
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ARTERIAL 20/40 MICRON FILTERS W/WO HEPARIN COATING is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Professionals, Inc.. It received FDA 510(k) clearance on 1987-01-02 under 510(k) number K864262. The device is classified under product code DTM. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTERIAL 20/40 MICRON FILTERS W/WO HEPARIN COATING?

ARTERIAL 20/40 MICRON FILTERS W/WO HEPARIN COATING is a medical device that received FDA 510(k) clearance on 1987-01-02. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K864262.

When did ARTERIAL 20/40 MICRON FILTERS W/WO HEPARIN COATING receive FDA 510(k) clearance?

ARTERIAL 20/40 MICRON FILTERS W/WO HEPARIN COATING received FDA 510(k) clearance on 1987-01-02, under 510(k) number K864262.

Who is the listed applicant for ARTERIAL 20/40 MICRON FILTERS W/WO HEPARIN COATING?

The FDA 510(k) record lists Johnson & Johnson Professionals, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ARTERIAL 20/40 MICRON FILTERS W/WO HEPARIN COATING?

The FDA product code for ARTERIAL 20/40 MICRON FILTERS W/WO HEPARIN COATING is DTM.

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 Johnson & Johnson Professionals, 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.

View all 206 devices →

Related Devices (Code: DTM)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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