ARTERIAL 20/40 MICRON FILTERS W/WO HEPARIN COATING
K-Number: K864262 · 1987-01-02
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Device Summary
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.
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
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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