510(k) Report

510(k) · Cleared

Cleared

SPOTFIRE VG Control Panel M534, SPOTFIRE VG Negative Control

K262573510(k) TraditionalCleared Oct 21, 202686-day reviewClass II21 CFR 866.3920

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

Maine Molecular Quality Controls, Inc. · PMN Assayed External Control Material For Microbiology Nucleic Acid Amplification (Nat) Assays

Cleared on Oct 21, 2026 after an 86-day review. FDA has not posted a summary or statement for it, so its predicates are not known.

Decided
Oct 21, 2026
Review
86 days
Class
Class II
Product code
PMN
Recalls
None
Predicates
0

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

FIG. 1 — Lineage of K262573Source: 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 PMN? 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 PMN device

  1. #1 K251526 FilmArray GI Control Panel M238score 13.7 · 4 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 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?

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 PMN devices

PMN Assayed External Control Material For Microbiology Nucleic Acid Amplification (Nat) Assays: FDA decisions, review times, recalls and adverse event reports over 20 years. 2026, this device’s year, is highlighted.

FDA decisions per year · PMN

1in 2025

2016: 32017: 22018: 32019: 62020: 22021: 12022: 32023: 42024: 22025: 12026 (partial year): 6
2007high 6 (2019) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · PMN

90in 2023

2018: 59 days median2019: 71 days median2022: 582 days median2023: 90 days median2026 (partial year): 85 days median
2007high 582 (2022) · low 59 (2018)2026

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

Recalls per year · PMN

1in 2019

2019: 1
2007high 1 (2019) · low 0 (2007)2026

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

Adverse event reports per year · PMN

1in 2023

2023: 1
2007high 1 (2023) · low 0 (2007)2025

MAUDE reports naming product code PMN, 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
20150—00
20163—00
20172—00
201835900
201967110
20202—00
20211—00
2022358200
202349001
20242—00
20251—00
20266850—
Cite this page

510(k) Report. “K262573: SPOTFIRE VG Control Panel M534, SPOTFIRE VG Negative Control.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K262573

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