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FDA 510(k)

EnteraLoc Flow

K-Number: K223683 · 2023-07-10

Decision Date2023-07-10
Product CodePIF
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

EnteraLoc Flow is the device name listed in this FDA 510(k) record. The listed applicant is Vonco Products. It received FDA 510(k) clearance on 2023-07-10 under 510(k) number K223683. 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 EnteraLoc Flow?

EnteraLoc Flow is a medical device that received FDA 510(k) clearance on 2023-07-10. The listed applicant is Vonco Products. The 510(k) number is K223683.

When did EnteraLoc Flow receive FDA 510(k) clearance?

EnteraLoc Flow received FDA 510(k) clearance on 2023-07-10, under 510(k) number K223683.

Who is the listed applicant for EnteraLoc Flow?

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

What is the FDA product code for EnteraLoc Flow?

The FDA product code for EnteraLoc Flow is PIF.

Other records listing Vonco 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.

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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