510(k) Report

FDA product code · Gastroenterology and urology

Tube, Nasogastric

BSSClass II21 CFR 876.5980510(k) required13 decisions since 19795 recalls

13 FDA decisions since 1979. 5 recalls name this code, 0 of them Class I. The most-cited predicate is K984629, named by 2 later devices.

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 BSS 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 · BSS

1in 2014

2014: 1
2007high 1 (2014) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · BSS

Too few BSS 510(k)s in any year since 2007 to give a median.

Recalls per year · BSS

5in 2023

2023: 5
2007high 5 (2023) · low 0 (2007)2026

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

Adverse event reports per year · BSS

10in 2025

2007: 12010: 22011: 22013: 12015: 42016: 12017: 92018: 92019: 142020: 62021: 82022: 222023: 272024: 142025: 10
2007high 27 (2023) · low 0 (2008)2025

MAUDE reports naming product code BSS, 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—01
20080—00
20090—00
20100—02
20110—02
20120—00
20130—01
20141—00
20150—04
20160—01
20170—09
20180—09
20190—014
20200—06
20210—08
20220—022
20230—527
20240—014
20250—010
20260—0—
FIG. 1 — BSS by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in BSS? 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.