510(k) Report

510(k) · Cleared

Cleared

Mobility+ Enteral Feeding System OTC

K233034510(k) TraditionalCleared Apr 12, 2024200-day reviewClass II21 CFR 876.5980

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Rockfield Medical · PIF Gastrointestinal Tubes With Enteral Specific Connectors

Cleared on Apr 12, 2024 as substantially equivalent to K222678 (Rockfield Medical, 2022) after a 200-day review. Its family tree reaches back 7 generations to 1985.

Decided
Apr 12, 2024
Review
200 days
Class
Class II
Product code
PIF
Recalls
None
Predicates
1

Its longest line of descent runs back 7 generations to K851539 (1985). 9 ancestors in all. No later device cites it as a predicate yet.

  1. Root · 7 generations backK851539 Chesebrough-Ponds Kangaroo Pump Set W/Easy-Cap CloChesebrough-Pond'S U.S.A. Co. · 1985
  2. 6 generations backK954735 EnteraliteZevex Intl., Inc. · 1996
  3. 5 generations backK012147 Device Modification of Enteral Feeding Sets for Gravity and Pump UseZevex, Inc. · 2001
  4. 4 generations backK082863 Dynarex Enteral Delivery Pump Set with Spike (1000ML), Dynarex…Dynarex Corporation · 2009
  5. 3 generations backK133077 Generica Medical Enternal Delivery; Pump Bag Set, Pump Spike Set…Generica Medical International, Inc. · 2014
  6. 2 generations backK150286 Medline Enteral Feeding SetsMedline Industries, Inc. · 2015
  7. 1 generation backK222678 Mobility+ Enteral Feeding SystemRockfield Medical · 2022
  8. This deviceK233034 Mobility+ Enteral Feeding System OTCRockfield Medical · 2024
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−7K851539Chesebrough-Ponds Kangaroo Pump Set W/Easy-Cap CloChesebrough-Pond'S U.S.A. Co.1985—
−6K954735EnteraliteZevex Intl., Inc.1996—
−5K012147Device Modification of Enteral Feeding Sets for Gravity and Pump UseZevex, Inc.2001—
−4K082863Dynarex Enteral Delivery Pump Set with Spike (1000ML), Dynarex Enteral Feeding…Dynarex Corporation2009—
−3K133077Generica Medical Enternal Delivery; Pump Bag Set, Pump Spike Set, Gravity Bag…Generica Medical International, Inc.2014—
−2K150286Medline Enteral Feeding SetsMedline Industries, Inc.2015—
−1K222678Mobility+ Enteral Feeding SystemRockfield Medical2022—
0 (this device)K233034Mobility+ Enteral Feeding System OTCRockfield Medical2024—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198610
199110
FIG. 1 — Lineage of K233034, 1985–2024Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in PIF? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new PIF device

  1. #1 K253715 Edi Catheter ENFit 6Fr/48 cm (6893166); Edi…score 15.5 · 13 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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What was it cleared against? (1)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K222678Mobility+ Enteral Feeding System
Summary page 6
…Page 2 of 4 Predicate Device Mobility+ Enteral Feeding System, K222678. Device Description The Mobility+ Enteral Feeding System OTC (“Mobility+ OTC” or the “System”) is a portable, lightweight, non…
Rockfield Medical2022—

What descends from it?

No later submission names this one as a predicate yet.

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 39 years and passes through 7 companies; a new generation was cleared every 5.5 years on median.
  • None of the 9 ancestors has a recall.

How does its category compare?

All PIF devices

PIF Gastrointestinal Tubes With Enteral Specific Connectors: FDA decisions, review times, recalls and adverse event reports over 20 years. 2024, this device’s year, is highlighted.

FDA decisions per year · PIF

2in 2025

2014: 32015: 92016: 32017: 52018: 22019: 72020: 42021: 42022: 42023: 42024: 22025: 22026 (partial year): 3
2007high 9 (2015) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · PIF

242in 2023

2014: 119 days median2015: 143 days median2016: 267 days median2017: 174 days median2019: 135 days median2020: 165 days median2021: 242 days median2022: 167 days median2023: 242 days median2026 (partial year): 239 days median
2007high 267 (2016) · low 119 (2014)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · PIF

1in 2024

2015: 1062024: 1
2007high 106 (2015) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · PIF

83in 2025

2015: 122016: 452017: 172018: 172019: 282020: 702021: 892022: 772023: 962024: 1102025: 83
2007high 110 (2024) · low 0 (2007)2025

MAUDE reports naming product code PIF, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—00
20080—00
20090—00
20100—00
20110—00
20120—00
20130—00
2014311900
2015914310612
20163267045
20175174017
20182—017
20197135028
20204165070
20214242089
20224167077
20234242096
20242—1110
20252—083
202632390—

What is it indicated for?

Mobility+ is intended to deliver liquid nutrition formula to an enteral access device (feeding tube) in users aged 2 years and over.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K233034: Mobility+ Enteral Feeding System OTC.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K233034

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026