Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Vesco Medical Extension Feeding Set

K-Number: K192991 · 2020-08-03

Decision Date2020-08-03
Product CodePIF
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Vesco Medical Extension Feeding Set is a medical device manufactured by Vesco Medical, LLC. It received FDA 510(k) clearance on 2020-08-03 under approval number K192991. 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 Vesco Medical Extension Feeding Set?

Vesco Medical Extension Feeding Set is a medical device that received FDA 510(k) clearance on 2020-08-03. It is manufactured by Vesco Medical, LLC. The 510(k) number is K192991.

When was Vesco Medical Extension Feeding Set approved by the FDA?

Vesco Medical Extension Feeding Set received FDA 510(k) clearance on 2020-08-03, under approval number K192991.

What company makes Vesco Medical Extension Feeding Set?

Vesco Medical Extension Feeding Set is manufactured by Vesco Medical, LLC.

What is the FDA product code for Vesco Medical Extension Feeding Set?

The FDA product code for Vesco Medical Extension Feeding Set is PIF.

Related Clinical Trials

Other Devices by Vesco Medical, LLC

Related Devices (Code: PIF)

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.