BREATHING CIRCUIT BACTERIAL FILTERS
K-Number: K892520 · 1989-08-02
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Device Summary
Frequently Asked Questions
What is the BREATHING CIRCUIT BACTERIAL FILTERS?
BREATHING CIRCUIT BACTERIAL FILTERS is a medical device that received FDA 510(k) clearance on 1989-08-02. The listed applicant is Arbo Medical, Inc.. The 510(k) number is K892520.
When did BREATHING CIRCUIT BACTERIAL FILTERS receive FDA 510(k) clearance?
BREATHING CIRCUIT BACTERIAL FILTERS received FDA 510(k) clearance on 1989-08-02, under 510(k) number K892520.
Who is the listed applicant for BREATHING CIRCUIT BACTERIAL FILTERS?
The FDA 510(k) record lists Arbo Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BREATHING CIRCUIT BACTERIAL FILTERS?
The FDA product code for BREATHING CIRCUIT BACTERIAL FILTERS 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 Arbo Medical, 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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