BREATHING FILTER
K-Number: K931842 · 1993-05-19
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Device Summary
Frequently Asked Questions
What is the BREATHING FILTER?
BREATHING FILTER is a medical device that received FDA 510(k) clearance on 1993-05-19. The listed applicant is Mag, Inc.. The 510(k) number is K931842.
When did BREATHING FILTER receive FDA 510(k) clearance?
BREATHING FILTER received FDA 510(k) clearance on 1993-05-19, under 510(k) number K931842.
Who is the listed applicant for BREATHING FILTER?
The FDA 510(k) record lists Mag, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BREATHING FILTER?
The FDA product code for BREATHING 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 Mag, 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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