510(k) Report

510(k) · Cleared

Cleared

Tina-Quant Microalbumin

K932950510(k) TraditionalCleared Feb 10, 1995603-day reviewClass I21 CFR 862.1645

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

Boehringer Mannheim Corp. · JIR Indicator Method, Protein Or Albumin (Urinary, Non-Quant.)

Cleared on Feb 10, 1995 after a 603-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 2 later devices descend from it.

Decided
Feb 10, 1995
Review
603 days
Class
Class I
Product code
JIR
Recalls
None
Predicates
0

2 later devices descend from it, 1 citing it directly.

Descendants, by year cleared 2010: 1 descendant cleared2012: 1 descendant cleared1995200020052010201520202025
  1. This deviceK932950 Tina-Quant MicroalbuminBoehringer Mannheim Corp. · 1995
  2. Descendant · cites it directly · 1 of its ownK101203 Tina-Quant Albumin Gen 2Roche Diagnostics · 2010 · Recalled
  3. Descendant · 2 generations on · 0 of its ownK113072 Tina-Quant Albumin Gen.2Roche Diagnostics Operations · 2012

Most influential descendants

Showing 2 of 2 · See all
  • K101203Tina-Quant Albumin Gen 2Roche Diagnostics · 2010 · cites it directly1descendant
  • K113072Tina-Quant Albumin Gen.2Roche Diagnostics Operations · 2012 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K932950Tina-Quant MicroalbuminBoehringer Mannheim Corp.1995—
+1K101203Tina-Quant Albumin Gen 2Roche Diagnostics20101
+2K113072Tina-Quant Albumin Gen.2Roche Diagnostics Operations2012—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201010
201210
FIG. 1 — Lineage of K932950, 1995–2012Source: 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), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in JIR? 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 JIR device

  1. #1 K210069 Minuteful - kidney testscore 7.5 · 4 generations · no Class I recall
  2. #2 Held for the reportin the report
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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? (2)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K101203Tina-Quant Albumin Gen 2Roche Diagnostics20101

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?

  • Of its descendants, K101203 (Roche Diagnostics, 2010) has gone furthest, with 1 descendant of its own.

How does its category compare?

All JIR devices

JIR Indicator Method, Protein Or Albumin (Urinary, Non-Quant.): FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · JIR

1in 2023

2007: 12015: 12022: 12023: 1
2007high 1 (2007) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · JIR

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

Recalls per year · JIR

2so far in 2026, the most since 2007

2026 (partial year): 2
2007high 2 (2026) · low 0 (2007)2026

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

Adverse event reports per year · JIR

2in 2025

2007: 12010: 12011: 12013: 92015: 42016: 52017: 22019: 12020: 22021: 12023: 22024: 42025: 2
2007high 9 (2013) · low 0 (2008)2025

MAUDE reports naming product code JIR, 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
20071—01
20080—00
20090—00
20100—01
20110—01
20120—00
20130—09
20140—00
20151—04
20160—05
20170—02
20180—00
20190—01
20200—02
20210—01
20221—00
20231—02
20240—04
20250—02
20260—2—
Cite this page

510(k) Report. “K932950: Tina-Quant Microalbumin.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K932950

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