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FDA 510(k)

Moss Gastrostomy Tube, Moss Nasal Tube – Mark IV

K-Number: K190414 · 2019-06-14

ApplicantMoss Tubes, Inc.
Decision Date2019-06-14
Product CodePIF
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Moss Gastrostomy Tube, Moss Nasal Tube – Mark IV is a medical device manufactured by Moss Tubes, Inc.. It received FDA 510(k) clearance on 2019-06-14 under approval number K190414. The device is classified under product code PIF. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Moss Gastrostomy Tube, Moss Nasal Tube – Mark IV?

Moss Gastrostomy Tube, Moss Nasal Tube – Mark IV is a medical device that received FDA 510(k) clearance on 2019-06-14. It is manufactured by Moss Tubes, Inc.. The 510(k) number is K190414.

When was Moss Gastrostomy Tube, Moss Nasal Tube – Mark IV approved by the FDA?

Moss Gastrostomy Tube, Moss Nasal Tube – Mark IV received FDA 510(k) clearance on 2019-06-14, under approval number K190414.

What company makes Moss Gastrostomy Tube, Moss Nasal Tube – Mark IV?

Moss Gastrostomy Tube, Moss Nasal Tube – Mark IV is manufactured by Moss Tubes, Inc..

What is the FDA product code for Moss Gastrostomy Tube, Moss Nasal Tube – Mark IV?

The FDA product code for Moss Gastrostomy Tube, Moss Nasal Tube – Mark IV is PIF.

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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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