510(k) Report

510(k) · Cleared

Cleared

Stat Profile Prime ES Comp Plus Analyzer System

K191626510(k) TraditionalCleared Aug 16, 201959-day reviewClass II21 CFR 862.1145

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

Nova Biomedical Corporation · JFP Electrode, Ion Specific, Calcium

Cleared on Aug 16, 2019 as substantially equivalent to K110648 (Nova Biomedical Corporation, 2011) after a 59-day review. Its family tree reaches back 2 generations to 2006.

Decided
Aug 16, 2019
Review
59 days
Class
Class II
Product code
JFP
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to K061830 (2006). No later device cites it as a predicate yet.

  1. Root · 2 generations backK061830 Stat Profile Critical Care Xpress (CCX), Model 1+Nova Biomedical Corp. · 2006
  2. 1 generation backK110648 Nova Stat Profile Phox Ultra Analyzer SystemNova Biomedical Corporation · 2011
  3. This deviceK191626 Stat Profile Prime ES Comp Plus Analyzer SystemNova Biomedical Corporation · 2019
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K061830Stat Profile Critical Care Xpress (CCX), Model 1+Nova Biomedical Corp.2006—
−1K110648Nova Stat Profile Phox Ultra Analyzer SystemNova Biomedical Corporation2011—
0 (this device)K191626Stat Profile Prime ES Comp Plus Analyzer SystemNova Biomedical Corporation2019—
FIG. 1 — Lineage of K191626, 2006–2019Source: 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), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in JFP? 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 JFP device

  1. #1 K230300 i-STAT CG8+ cartridge with the i-STAT 1 Systemscore 6.8 · 3 generations · no Class I recall
  2. #2 Held for the reportin the report
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What was it cleared against? (1)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K110648Nova Stat Profile Phox Ultra Analyzer System
Summary page 4
…II CHL Hematocrit Test System 864.6400 II GKF Hematology (81) Product Codes: CHL, JFP, CFA, GKF Predicate Devices: K110648 - Nova Stat Profile pHOx Ultra Blood Gas Analyzer Device Description: The Stat Profile Prime ES Comp Plus Analyzer is a small,…
Nova Biomedical Corporation2011—

Also cleared against K110648: 8 other devices →

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.

What does this lineage say?

  • The line of descent spans 13 years and passes through 2 companies; a new generation was cleared every 8.0 years on median.
  • None of the 2 ancestors has a recall.
  • 8 other devices also cite its predicate K110648.

How does its category compare?

All JFP devices

JFP Electrode, Ion Specific, Calcium: FDA decisions, review times, recalls and adverse event reports over 20 years. 2019, this device’s year, is highlighted.

FDA decisions per year · JFP

1in 2023

2016: 12019: 12020: 12023: 1
2007high 1 (2016) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · JFP

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

Recalls per year · JFP

1in 2011

2008: 12011: 1
2007high 1 (2008) · low 0 (2007)2026

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

Adverse event reports per year · JFP

40in 2025

2008: 52009: 52010: 22011: 82013: 12014: 12015: 32017: 22018: 52019: 62020: 62022: 62023: 22024: 82025: 40
2007high 40 (2025) · low 0 (2007)2025

MAUDE reports naming product code JFP, 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—15
20090—05
20100—02
20110—18
20120—00
20130—01
20140—01
20150—03
20161—00
20170—02
20180—05
20191—06
20201—06
20210—00
20220—06
20231—02
20240—08
20250—040
20260—0—

What is it indicated for?

The Stat Profile Prime ES Comp Plus Analyzer System is intended for in vitro diagnostic use by health care professionals in clinical laboratory settings for the quantitative determination of pH, Hematocrit, Ionized Calcium and Ionized Magnesium in heparinized venous whole blood, and pH, Ionized Calcium and Ionized Magnesium in plasma and serum. Ionized Calcium (iCa) measurements are used in the diagnosis and treatment of parathyroid disease, a variety of…

Read the full statement (141 words)

The Stat Profile Prime ES Comp Plus Analyzer System is intended for in vitro diagnostic use by health care professionals in clinical laboratory settings for the quantitative determination of pH, Hematocrit, Ionized Calcium and Ionized Magnesium in heparinized venous whole blood, and pH, Ionized Calcium and Ionized Magnesium in plasma and serum.

Ionized Calcium (iCa) measurements are used in the diagnosis and treatment of parathyroid disease, a variety of bone diseases, chronic renal disease and tetany (intermittent muscular contractions or spasms).

Ionized Magnesium (iMg) measurements are used in the diagnosis and treatment of hypomagnesemia (abnormally low levels of magnesium) and hypermagnesemia (abnormally high levels of magnesium).

pH measurements are used in the diagnosis and treatment of life-threatening acid-base disturbances.

Hematocrit measurements of the packed red blood cell volume are used to distinguish normal from abnormal states, such as anemia and erythrocytosis.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K191626: Stat Profile Prime ES Comp Plus Analyzer System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K191626

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026