Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

SILICONE RUBBER-BI NASOPHARYNGEAL AIR

K-Number: K792018 · 1979-11-13

ApplicantVesta, Inc.
Decision Date1979-11-13
Product CodeBTQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SILICONE RUBBER-BI NASOPHARYNGEAL AIR is the device name listed in this FDA 510(k) record. The listed applicant is Vesta, Inc.. It received FDA 510(k) clearance on 1979-11-13 under 510(k) number K792018. The device is classified under product code BTQ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

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.

↑