RESUBMITTED MICRON TRANSFUSION FILTER
K-Number: K873873 · 1987-10-22
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Device Summary
Frequently Asked Questions
What is the RESUBMITTED MICRON TRANSFUSION FILTER?
RESUBMITTED MICRON TRANSFUSION FILTER is a medical device that received FDA 510(k) clearance on 1987-10-22. The listed applicant is Travenol Laboratories, S.A.. The 510(k) number is K873873.
When did RESUBMITTED MICRON TRANSFUSION FILTER receive FDA 510(k) clearance?
RESUBMITTED MICRON TRANSFUSION FILTER received FDA 510(k) clearance on 1987-10-22, under 510(k) number K873873.
Who is the listed applicant for RESUBMITTED MICRON TRANSFUSION FILTER?
The FDA 510(k) record lists Travenol Laboratories, S.A. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RESUBMITTED MICRON TRANSFUSION FILTER?
The FDA product code for RESUBMITTED MICRON TRANSFUSION FILTER is CAK.
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 Travenol Laboratories, S.A. 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: CAK)
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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