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FDA 510(k)

MOSS NASAL TUBE MARK IV

K-Number: K910912 · 1991-05-28

Decision Date1991-05-28
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MOSS NASAL TUBE MARK IV is the device name listed in this FDA 510(k) record. The listed applicant is Moss Medical Products. It received FDA 510(k) clearance on 1991-05-28 under 510(k) number K910912. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOSS NASAL TUBE MARK IV?

MOSS NASAL TUBE MARK IV is a medical device that received FDA 510(k) clearance on 1991-05-28. The listed applicant is Moss Medical Products. The 510(k) number is K910912.

When did MOSS NASAL TUBE MARK IV receive FDA 510(k) clearance?

MOSS NASAL TUBE MARK IV received FDA 510(k) clearance on 1991-05-28, under 510(k) number K910912.

Who is the listed applicant for MOSS NASAL TUBE MARK IV?

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

What is the FDA product code for MOSS NASAL TUBE MARK IV?

The FDA product code for MOSS NASAL TUBE MARK IV is KNT.

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 Moss Medical Products 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 8 devices →

Related Devices (Code: KNT)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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