510(k) Report

510(k) · Cleared

Cleared

FlowMet-R

K182494510(k) TraditionalCleared Feb 27, 2019169-day reviewClass II21 CFR 870.2100

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

Laser Associated Sciences, Inc. · DPW Flowmeter, Blood, Cardiovascular

Cleared on Feb 27, 2019 as substantially equivalent to K120884 (Perimed AB, 2012) after a 169-day review. Its family tree reaches back 5 generations to 1991. 1 later device descends from it.

Decided
Feb 27, 2019
Review
169 days
Class
Class II
Product code
DPW
Recalls
None
Predicates
1

Its longest line of descent runs back 5 generations to K905232 (1991). 6 ancestors in all. 1 later device descends from it, 1 citing it directly.

  1. Root · 5 generations backK905232 Moor Laser Blood Flow Monitor MBF3Moor Instruments, Ltd. · 1991
  2. 4 generations backK980383 Mooorldi Laser Doppler ImagerMoor Instruments, Ltd. · 1998
  3. 3 generations backK032841 Moorldi Infrared Laser Doppler Imager, Model MOORLD12-IRMoor Instruments, Ltd. · 2003
  4. 2 generations backK063586 Moorflpi Full-Field Laser Perfusion ImagerMoor Instruments, Ltd. · 2007
  5. 1 generation backK120884 Pericam PsiPerimed AB · 2012
  6. This deviceK182494 FlowMet-RLaser Associated Sciences, Inc. · 2019
  7. Descendant · cites it directly · 0 of its ownK192966 FlowMetLaser Associated Sciences, Inc. · 2020

Most influential descendants

Showing 1 of 1 · See all
  • K192966FlowMetLaser Associated Sciences, Inc. · 2020 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−5K905232Moor Laser Blood Flow Monitor MBF3Moor Instruments, Ltd.1991—
−4K980383Mooorldi Laser Doppler ImagerMoor Instruments, Ltd.1998—
−3K032841Moorldi Infrared Laser Doppler Imager, Model MOORLD12-IRMoor Instruments, Ltd.2003—
−2K063586Moorflpi Full-Field Laser Perfusion ImagerMoor Instruments, Ltd.2007—
−1K120884Pericam PsiPerimed AB2012—
0 (this device)K182494FlowMet-RLaser Associated Sciences, Inc.2019—
+1K192966FlowMetLaser Associated Sciences, Inc.2020—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199210

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202010
FIG. 1 — Lineage of K182494, 1991–2020Source: 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 DPW? 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 DPW device

  1. #1 K251114 FloPatch FP120score 13.7 · 5 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

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
*K120884Pericam Psi
Summary page 4
…e Device Information Trade name: PeriCam PSI Model No: PeriCam PSI NR, PeriCam PSI HR 510(k) No: K120884 Type of product: Finished product Panel: Cardiovascular Common Name:…
Perimed AB2012—
†K974285Periflux System 5000 Modular Laser Doppler System Main Unit Model PF 5001, Including PF…Perimed, Inc.1998—

Also cleared against K120884: 1 other device →

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K192966FlowMetLaser Associated Sciences, Inc.20200

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 28 years and passes through 3 companies; a new generation was cleared every 5.6 years on median.
  • None of the 6 ancestors has a recall.
  • Of its descendants, K192966 (Laser Associated Sciences, Inc., 2020) has gone furthest, with 0 descendants of its own.
  • 1 other device also cites its predicate K120884.

How does its category compare?

All DPW devices

DPW Flowmeter, Blood, Cardiovascular: FDA decisions, review times, recalls and adverse event reports over 20 years. 2019, this device’s year, is highlighted.

FDA decisions per year · DPW

3in 2025

2007: 12008: 12010: 22011: 42012: 12013: 22015: 32016: 12018: 22019: 32020: 22021: 22022: 32023: 12024: 12025: 32026 (partial year): 2
2007high 4 (2011) · low 0 (2009)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · DPW

119in 2025

2011: 89 days median2015: 275 days median2019: 169 days median2022: 136 days median2025: 119 days median
2007high 275 (2015) · low 89 (2011)2026

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

Recalls per year · DPW

1in 2025

2007: 42010: 12012: 12017: 12025: 1
2007high 4 (2007) · low 0 (2008)2026

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

Adverse event reports per year · DPW

6in 2025

2009: 12011: 12013: 32014: 82015: 122016: 12017: 22019: 32020: 42021: 62022: 12023: 22024: 42025: 6
2007high 12 (2015) · low 0 (2007)2025

MAUDE reports naming product code DPW, 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—40
20081—00
20090—01
20102—10
201148901
20121—10
20132—03
20140—08
20153275012
20161—01
20170—12
20182—00
2019316903
20202—04
20212—06
2022313601
20231—02
20241—04
2025311916
20262—0—

What is it indicated for?

The FlowMet-R is a non-invasive probe that is affixed to the fingers or toes and intended to quantify tissue blood flow rate.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K182494: FlowMet-R.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K182494

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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