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FDA 510(k)

Mobility+ Enteral Feeding System

K-Number: K222678 · 2022-10-27

Decision Date2022-10-27
Product CodePIF
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Mobility+ Enteral Feeding System is the device name listed in this FDA 510(k) record. The listed applicant is Rockfield Medical. It received FDA 510(k) clearance on 2022-10-27 under 510(k) number K222678. 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 Mobility+ Enteral Feeding System?

Mobility+ Enteral Feeding System is a medical device that received FDA 510(k) clearance on 2022-10-27. The listed applicant is Rockfield Medical. The 510(k) number is K222678.

When did Mobility+ Enteral Feeding System receive FDA 510(k) clearance?

Mobility+ Enteral Feeding System received FDA 510(k) clearance on 2022-10-27, under 510(k) number K222678.

Who is the listed applicant for Mobility+ Enteral Feeding System?

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

What is the FDA product code for Mobility+ Enteral Feeding System?

The FDA product code for Mobility+ Enteral Feeding System is PIF.

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