UNIPOR BREATHING CIRCUIT FILTER
K-Number: K791307 · 1979-08-03
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Device Summary
Frequently Asked Questions
What is the UNIPOR BREATHING CIRCUIT FILTER?
UNIPOR BREATHING CIRCUIT FILTER is a medical device that received FDA 510(k) clearance on 1979-08-03. The listed applicant is Pall Biomedical Products Co.. The 510(k) number is K791307.
When did UNIPOR BREATHING CIRCUIT FILTER receive FDA 510(k) clearance?
UNIPOR BREATHING CIRCUIT FILTER received FDA 510(k) clearance on 1979-08-03, under 510(k) number K791307.
Who is the listed applicant for UNIPOR BREATHING CIRCUIT FILTER?
The FDA 510(k) record lists Pall Biomedical Products Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for UNIPOR BREATHING CIRCUIT FILTER?
The FDA product code for UNIPOR BREATHING CIRCUIT FILTER is CAH.
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 Pall Biomedical Products Co. 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: CAH)
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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