SILICONE RUBBER-BI NASOPHARYNGEAL AIR
K-Number: K792018 · 1979-11-13
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Device Summary
Frequently Asked Questions
What is the SILICONE RUBBER-BI NASOPHARYNGEAL AIR?
SILICONE RUBBER-BI NASOPHARYNGEAL AIR is a medical device that received FDA 510(k) clearance on 1979-11-13. The listed applicant is Vesta, Inc.. The 510(k) number is K792018.
When did SILICONE RUBBER-BI NASOPHARYNGEAL AIR receive FDA 510(k) clearance?
SILICONE RUBBER-BI NASOPHARYNGEAL AIR received FDA 510(k) clearance on 1979-11-13, under 510(k) number K792018.
Who is the listed applicant for SILICONE RUBBER-BI NASOPHARYNGEAL AIR?
The FDA 510(k) record lists Vesta, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SILICONE RUBBER-BI NASOPHARYNGEAL AIR?
The FDA product code for SILICONE RUBBER-BI NASOPHARYNGEAL AIR is BTQ.
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 Vesta, 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: BTQ)
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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