FILT-R-ALL BACTERIAL/VIRAL FILTER
K-Number: K900990 · 1990-04-19
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Device Summary
Frequently Asked Questions
What is the FILT-R-ALL BACTERIAL/VIRAL FILTER?
FILT-R-ALL BACTERIAL/VIRAL FILTER is a medical device that received FDA 510(k) clearance on 1990-04-19. The listed applicant is Inhalation Plastics. The 510(k) number is K900990.
When did FILT-R-ALL BACTERIAL/VIRAL FILTER receive FDA 510(k) clearance?
FILT-R-ALL BACTERIAL/VIRAL FILTER received FDA 510(k) clearance on 1990-04-19, under 510(k) number K900990.
Who is the listed applicant for FILT-R-ALL BACTERIAL/VIRAL FILTER?
The FDA 510(k) record lists Inhalation Plastics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FILT-R-ALL BACTERIAL/VIRAL FILTER?
The FDA product code for FILT-R-ALL BACTERIAL/VIRAL 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 Inhalation Plastics 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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