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FDA 510(k)

Mobility+ Enteral Feeding System

K-Number: K222678 · 2022-10-27

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

Device Summary

Mobility+ Enteral Feeding System is a medical device manufactured by Rockfield Medical. It received FDA 510(k) clearance on 2022-10-27 under approval 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. It is manufactured by Rockfield Medical. The 510(k) number is K222678.

When was Mobility+ Enteral Feeding System approved by the FDA?

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

What company makes Mobility+ Enteral Feeding System?

Mobility+ Enteral Feeding System is manufactured by Rockfield Medical.

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

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

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Other Devices by Rockfield Medical

K233034Mobility+ Enteral Feeding System OTC

Related Devices (Code: 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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