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FDA 510(k)

FRANCIS NASAL TUBE

K-Number: K822130 · 1982-10-13

ApplicantTekna Med Corp.
Decision Date1982-10-13
Product CodeFZE
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FRANCIS NASAL TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Tekna Med Corp.. It received FDA 510(k) clearance on 1982-10-13 under 510(k) number K822130. The device is classified under product code FZE. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FRANCIS NASAL TUBE?

FRANCIS NASAL TUBE is a medical device that received FDA 510(k) clearance on 1982-10-13. The listed applicant is Tekna Med Corp.. The 510(k) number is K822130.

When did FRANCIS NASAL TUBE receive FDA 510(k) clearance?

FRANCIS NASAL TUBE received FDA 510(k) clearance on 1982-10-13, under 510(k) number K822130.

Who is the listed applicant for FRANCIS NASAL TUBE?

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

What is the FDA product code for FRANCIS NASAL TUBE?

The FDA product code for FRANCIS NASAL TUBE is FZE.

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Related Devices (Code: FZE)

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.

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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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