POROUS MEDIA DBF23 DISPOSABLE RESPIRATORY FILTER
K-Number: K964979 · 1997-03-11
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Device Summary
Frequently Asked Questions
What is the POROUS MEDIA DBF23 DISPOSABLE RESPIRATORY FILTER?
POROUS MEDIA DBF23 DISPOSABLE RESPIRATORY FILTER is a medical device that received FDA 510(k) clearance on 1997-03-11. The listed applicant is Porous Media Corp.. The 510(k) number is K964979.
When did POROUS MEDIA DBF23 DISPOSABLE RESPIRATORY FILTER receive FDA 510(k) clearance?
POROUS MEDIA DBF23 DISPOSABLE RESPIRATORY FILTER received FDA 510(k) clearance on 1997-03-11, under 510(k) number K964979.
Who is the listed applicant for POROUS MEDIA DBF23 DISPOSABLE RESPIRATORY FILTER?
The FDA 510(k) record lists Porous Media Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POROUS MEDIA DBF23 DISPOSABLE RESPIRATORY FILTER?
The FDA product code for POROUS MEDIA DBF23 DISPOSABLE RESPIRATORY 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 Porous Media Corp. 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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