AVITA NASAL ASPIRATOR, MODEL, NS1 SERIES
K-Number: K090379 · 2010-05-26
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Device Summary
Frequently Asked Questions
What is the AVITA NASAL ASPIRATOR, MODEL, NS1 SERIES?
AVITA NASAL ASPIRATOR, MODEL, NS1 SERIES is a medical device that received FDA 510(k) clearance on 2010-05-26. The listed applicant is Avita Corporation. The 510(k) number is K090379.
When did AVITA NASAL ASPIRATOR, MODEL, NS1 SERIES receive FDA 510(k) clearance?
AVITA NASAL ASPIRATOR, MODEL, NS1 SERIES received FDA 510(k) clearance on 2010-05-26, under 510(k) number K090379.
Who is the listed applicant for AVITA NASAL ASPIRATOR, MODEL, NS1 SERIES?
The FDA 510(k) record lists Avita Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AVITA NASAL ASPIRATOR, MODEL, NS1 SERIES?
The FDA product code for AVITA NASAL ASPIRATOR, MODEL, NS1 SERIES is BTA.
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 Avita Corporation 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: BTA)
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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