510(k) Report

FDA product code · Gastroenterology and urology

Enteral Syringes With Enteral Specific Connectors

PNRClass II21 CFR 876.5980510(k) required35 decisions since 20154 recalls

35 FDA decisions since 2015. 510(k) reviews decided 2021–2025 took a median of 129 days (half between 58 and 241). 4 recalls name this code, 4 of them Class I. The most-cited predicate is K161039, named by 10 later devices.

Delivers nutrition, medication, or hydration orally or to a gastrointestinal tube or extension set using AAMI/CN3(PS):2014 compliant connectors.

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

FIG. A — Illustration, gastroenterology and urology panel

Twenty years of PNR at a glance: how often FDA decides these devices, how long 510(k) reviews take, how often they are recalled, and how many adverse event reports name the code.

FDA decisions per year · PNR

1in 2025

2015: 32016: 62017: 52018: 32019: 22020: 32021: 52022: 22023: 22024: 12025: 12026 (partial year): 2
2007high 6 (2016) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · PNR

129in 2021

2015: 139 days median2016: 65 days median2017: 247 days median2018: 133 days median2020: 209 days median2021: 129 days median
2007high 247 (2017) · low 65 (2016)2026

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

Recalls per year · PNR

4in 2023

2023: 4, 4 Class I
2007high 4 (2023) · low 0 (2007)2026

Class I (4 since 2007) Class II/III not classified

Adverse event reports per year · PNR

7in 2025

2016: 12017: 32018: 22019: 82020: 32021: 52022: 22023: 112024: 342025: 7
2007high 34 (2024) · low 0 (2007)2025

MAUDE reports naming product code PNR, 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
20140—00
2015313900
201666501
2017524703
2018313302
20192—08
2020320903
2021512905
20222—02
20232—4 (4)11
20241—034
20251—07
20262—0—
FIG. 1 — PNR by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in PNR? A 510(k) Report ranks candidate predicates in this code by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Related product codes

Other codes under 21 CFR 876.5980.