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FDA 510(k)

Moss Gastrostomy Tube, Moss Nasal Tube – Mark IV

K-Number: K190414 · 2019-06-14

Decision Date2019-06-14
Product CodePIF
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Moss Gastrostomy Tube, Moss Nasal Tube – Mark IV is the device name listed in this FDA 510(k) record. The listed applicant is Moss Tubes, Inc.. It received FDA 510(k) clearance on 2019-06-14 under 510(k) 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. The listed applicant is Moss Tubes, Inc.. The 510(k) number is K190414.

When did Moss Gastrostomy Tube, Moss Nasal Tube – Mark IV receive FDA 510(k) clearance?

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

Who is the listed applicant for Moss Gastrostomy Tube, Moss Nasal Tube – Mark IV?

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

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.

Related Devices (Code: PIF)

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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