510(k) Report

510(k) · Cleared

Recalled · 2003

Vitaflow Suction/Aspiration Tubing Set

K960616510(k) TraditionalCleared May 6, 199683-day reviewClass II21 CFR 880.6740Recalls 6

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

Vital Concepts, Inc. · BYY Tube, Aspirating, Flexible, Connecting

Cleared on May 6, 1996 after an 83-day review. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known. It has been recalled 6 times.

Decided
May 6, 1996
Review
83 days
Class
Class II
Product code
BYY
Recalls
6
Predicates
0

FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

FIG. 1 — Lineage of K960616Source: 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.

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

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  • Recall history across each candidate’s familyin the report
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What was it cleared against?

FDA lists a 510(k) statement for it but has not posted the file, 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)

Recalls of this device

DateClassRecallRoot causeReason
Jul 11, 2003Not classifiedZ-0022-04OtherThe suction valve may become stuck in the 'suction on' position under vacuum.
Jul 11, 2003Not classifiedZ-0025-04OtherThe suction valve may become stuck in the 'suction on' position under vacuum.
Jul 11, 2003Not classifiedZ-0020-04OtherThe suction valve may become stuck in the 'suction on' position under vacuum.
Jul 11, 2003Not classifiedZ-0021-04OtherThe suction valve may become stuck in the 'suction on' position under vacuum.
Jul 11, 2003Not classifiedZ-0023-04OtherThe suction valve may become stuck in the 'suction on' position under vacuum.
Jul 11, 2003Not classifiedZ-0024-04OtherThe suction valve may become stuck in the 'suction on' position under vacuum.

No ancestor or descendant has a Class I recall.

How does its category compare?

All BYY devices

BYY Tube, Aspirating, Flexible, Connecting: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · BYY

FDA has decided no BYY device since 2007.

Median 510(k) review, days · BYY

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

Recalls per year · BYY

1in 2008

2008: 1
2007high 1 (2008) · low 0 (2007)2026

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

Adverse event reports per year · BYY

14in 2025

2009: 42010: 22011: 12013: 52014: 32015: 22016: 202017: 342018: 122019: 182020: 232021: 112022: 112023: 112024: 32025: 14
2007high 34 (2017) · low 0 (2007)2025

MAUDE reports naming product code BYY, 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—10
20090—04
20100—02
20110—01
20120—00
20130—05
20140—03
20150—02
20160—020
20170—034
20180—012
20190—018
20200—023
20210—011
20220—011
20230—011
20240—03
20250—014
20260—0—
Cite this page

510(k) Report. “K960616: Vitaflow Suction/Aspiration Tubing Set.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K960616

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