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FDA 510(k)

INSTANT IN-DWELL NASAL SUCT TAMP/ALLEVIA NASAL TRA

K-Number: K924944 · 1993-07-02

ApplicantWestmed Intl.
Decision Date1993-07-02
Product CodeEMX
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

INSTANT IN-DWELL NASAL SUCT TAMP/ALLEVIA NASAL TRA is the device name listed in this FDA 510(k) record. The listed applicant is Westmed Intl.. It received FDA 510(k) clearance on 1993-07-02 under 510(k) number K924944. The device is classified under product code EMX. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INSTANT IN-DWELL NASAL SUCT TAMP/ALLEVIA NASAL TRA?

INSTANT IN-DWELL NASAL SUCT TAMP/ALLEVIA NASAL TRA is a medical device that received FDA 510(k) clearance on 1993-07-02. The listed applicant is Westmed Intl.. The 510(k) number is K924944.

When did INSTANT IN-DWELL NASAL SUCT TAMP/ALLEVIA NASAL TRA receive FDA 510(k) clearance?

INSTANT IN-DWELL NASAL SUCT TAMP/ALLEVIA NASAL TRA received FDA 510(k) clearance on 1993-07-02, under 510(k) number K924944.

Who is the listed applicant for INSTANT IN-DWELL NASAL SUCT TAMP/ALLEVIA NASAL TRA?

The FDA 510(k) record lists Westmed Intl. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INSTANT IN-DWELL NASAL SUCT TAMP/ALLEVIA NASAL TRA?

The FDA product code for INSTANT IN-DWELL NASAL SUCT TAMP/ALLEVIA NASAL TRA is EMX.

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 Westmed Intl. 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.

View all 9 devices →

Related Devices (Code: EMX)

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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