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FDA 510(k)

FOX POST NASAL BALLOON CATHETER

K-Number: K841040 · 1984-08-17

ApplicantInmed Corp.
Decision Date1984-08-17
Product CodeEMX
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

FOX POST NASAL BALLOON CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Inmed Corp.. It received FDA 510(k) clearance on 1984-08-17 under 510(k) number K841040. 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 FOX POST NASAL BALLOON CATHETER?

FOX POST NASAL BALLOON CATHETER is a medical device that received FDA 510(k) clearance on 1984-08-17. The listed applicant is Inmed Corp.. The 510(k) number is K841040.

When did FOX POST NASAL BALLOON CATHETER receive FDA 510(k) clearance?

FOX POST NASAL BALLOON CATHETER received FDA 510(k) clearance on 1984-08-17, under 510(k) number K841040.

Who is the listed applicant for FOX POST NASAL BALLOON CATHETER?

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

What is the FDA product code for FOX POST NASAL BALLOON CATHETER?

The FDA product code for FOX POST NASAL BALLOON CATHETER 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 Inmed Corp. 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 32 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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