510(k) Report

510(k) · Cleared

Cleared

Hemosil Protein S Activity Assay

K102164510(k) TraditionalCleared Mar 17, 2011227-day reviewClass II21 CFR 864.7290

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

Instrumentation Laboratory CO · GGP Test, Qualitative And Quantitative Factor Deficiency

Cleared on Mar 17, 2011 as substantially equivalent to K053499 (Instrumentation Laboratory CO, 2006) after a 227-day review. Its family tree reaches back 2 generations to 2001.

Decided
Mar 17, 2011
Review
227 days
Class
Class II
Product code
GGP
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to K011424 (2001). No later device cites it as a predicate yet.

  1. Root · 2 generations backK011424 IL Test ProsInstrumentation Laboratory CO · 2001
  2. 1 generation backK053499 Hemosil ProsInstrumentation Laboratory CO · 2006
  3. This deviceK102164 Hemosil Protein S Activity AssayInstrumentation Laboratory CO · 2011
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K011424IL Test ProsInstrumentation Laboratory CO2001—
−1K053499Hemosil ProsInstrumentation Laboratory CO2006—
0 (this device)K102164Hemosil Protein S Activity AssayInstrumentation Laboratory CO2011—
FIG. 1 — Lineage of K102164, 2001–2011Source: 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 GGP? 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 GGP device

  1. #1 K251440 CRYOcheck Chromogenic Factor VIIIscore 10.5 · 3 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? (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
*K053499Hemosil Pros
Summary page 2
…tics of the Device Similarities The H-emoslL Protein S Activity Assay is Substantially Equivalent to its predicate, the HemosiL ProS Assay (K053499), in both intended use and performance: TABLE 1: TABLE OF SIMII.ARIT AND DIFFERENCES Item…
Instrumentation Laboratory CO2006—

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 10 years and passes through 1 company; a new generation was cleared every 5.2 years on median.
  • None of the 2 ancestors has a recall.

How does its category compare?

All GGP devices

GGP Test, Qualitative And Quantitative Factor Deficiency: FDA decisions, review times, recalls and adverse event reports over 20 years. 2011, this device’s year, is highlighted.

FDA decisions per year · GGP

1in 2025

2007: 32008: 22009: 12011: 12014: 12018: 12019: 12020: 22022: 22023: 22025: 1
2007high 3 (2007) · low 0 (2010)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · GGP

153in 2007

2007: 153 days median
2007high 153 (2007)2026

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

Recalls per year · GGP

1in 2017

2007: 22010: 12012: 22015: 22017: 12026 (partial year): 1
2007high 2 (2007) · low 0 (2008)2026

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

Adverse event reports per year · GGP

3in 2025

2012: 42014: 12015: 12017: 32018: 32019: 12021: 22022: 42025: 3
2007high 4 (2012) · low 0 (2007)2025

MAUDE reports naming product code GGP, 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
2007315320
20082—00
20091—00
20100—10
20111—00
20120—24
20130—00
20141—01
20150—21
20160—00
20170—13
20181—03
20191—01
20202—00
20210—02
20222—04
20232—00
20240—00
20251—03
20260—1—

What is it indicated for?

Automated coagulation functional assay for the quantitative determination of free Protein S

in human citrated plasma as an aid in the diagnosis of hereditary and acquired Protein S

deficiency, on the ACL TOP Family of analyzers.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K102164: Hemosil Protein S Activity Assay.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K102164

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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