BREATHING CIRCUIT FILTER
K-Number: K012958 · 2002-02-22
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Device Summary
Frequently Asked Questions
What is the BREATHING CIRCUIT FILTER?
BREATHING CIRCUIT FILTER is a medical device that received FDA 510(k) clearance on 2002-02-22. The listed applicant is Emergency Filtration Products, Inc.. The 510(k) number is K012958.
When did BREATHING CIRCUIT FILTER receive FDA 510(k) clearance?
BREATHING CIRCUIT FILTER received FDA 510(k) clearance on 2002-02-22, under 510(k) number K012958.
Who is the listed applicant for BREATHING CIRCUIT FILTER?
The FDA 510(k) record lists Emergency Filtration Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BREATHING CIRCUIT FILTER?
The FDA product code for 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 Emergency Filtration Products, 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: 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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