510(k) Report

510(k) · Cleared

Cleared

Bard (R) Surecatch Pediatric Urine Collect Device

K911329510(k) TraditionalCleared May 28, 199163-day reviewClass II21 CFR 876.5250

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

C.R. Bard, Inc. · FOC Bag, Urine Collection, Newborn

Cleared on May 28, 1991 after a 63-day review. FDA has not posted a summary or statement for it, so its predicates are not known.

Decided
May 28, 1991
Review
63 days
Class
Class II
Product code
FOC
Recalls
None
Predicates
0

FDA has not posted a summary or statement for it, so its predicates are not known.

FIG. 1 — Lineage of K911329Source: FDA 510(k) database · 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), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

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What was it cleared against?

FDA has not posted a summary or statement for it, so its predicates are not known.

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.

How does its category compare?

All FOC devices

FOC Bag, Urine Collection, Newborn: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · FOC

FDA has decided no FOC device since 2007.

Median 510(k) review, days · FOC

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

Recalls per year · FOC

No recall names FOC since 2007.

Adverse event reports per year · FOC

No MAUDE report names FOC since 2007.

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
20150—00
20160—00
20170—00
20180—00
20190—00
20200—00
20210—00
20220—00
20230—00
20240—00
20250—00
20260—0—
Cite this page

510(k) Report. “K911329: Bard (R) Surecatch Pediatric Urine Collect Device.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K911329

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Record history
  • FDA decision record loaded May 2, 2026
  • Page last updated Nov 3, 2026