510(k) Report

510(k) · Cleared

Cleared

Digiflo Concentrator Analyzer

K072469510(k) TraditionalCleared Jan 3, 2008121-day reviewClass II21 CFR 868.1720

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

Digiflo, Inc. · CCL Analyzer, Gas, Oxygen, Gaseous-Phase

Cleared on Jan 3, 2008 as substantially equivalent to K984295 (Invacare Corp., 1999) and 1 other predicate after a 121-day review. Its family tree reaches back 2 generations to 1992. 3 later devices descend from it.

Decided
Jan 3, 2008
Review
121 days
Class
Class II
Product code
CCL
Recalls
None
Predicates
2

Its longest line of descent runs back 2 generations to K920338 (1992). 3 ancestors in all. 3 later devices descend from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 1999: 1 other ancestor2011: 1 descendant cleared2025: 1 descendant cleared2026: 1 descendant clearedK920338 · Companion Retrofit Oxygen Concentration Indicator · Puritan Bennett Corp. · 1992K984295 · Invacare Check O2 Plus Concentrator Analyzer (Check O2 Plus) · Invacare Corp. · 19991990200020102020
Other ancestors, by generationDescendants, by generation 1 generation back: 1 other ancestor 1 generation forward: 1 descendant2 generations forward: 2 descendants K984295 · Invacare Check O2 Plus Concentrator Analyzer (Check O2 Plus) · Invacare Corp. · 1999K920338 · Companion Retrofit Oxygen Concentration Indicator · Puritan Bennett Corp. · 19920
  1. Root · 2 generations backK920338 Companion Retrofit Oxygen Concentration IndicatorPuritan Bennett Corp. · 1992
  2. 1 generation backK984295 Invacare Check O2 Plus Concentrator Analyzer (Check O2 Plus)Invacare Corp. · 1999
  3. This deviceK072469 Digiflo Concentrator AnalyzerDigiflo, Inc. · 2008
  4. Descendant · cites it directly · 2 of its ownK112402 ULTRAMAXO2 Oxygen AnalyerMaxtec, LLC · 2011
  5. Descendant · 2 generations on · 0 of its ownK261389 PRO2 Elite Plus Oxygen Analyzer (PRO2PLUS-1)Salter Labs · 2026
  6. Descendant · 2 generations on · 0 of its ownK250002 Smart Check O2 (MA0236)Life Spark Medical, LLC · 2025

Most influential descendants

Showing 3 of 3 · See all
  • K112402ULTRAMAXO2 Oxygen AnalyerMaxtec, LLC · 2011 · cites it directly2descendants
  • K261389PRO2 Elite Plus Oxygen Analyzer (PRO2PLUS-1)Salter Labs · 2026 · 2 generations on0descendants
  • K250002Smart Check O2 (MA0236)Life Spark Medical, LLC · 2025 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K920338Companion Retrofit Oxygen Concentration IndicatorPuritan Bennett Corp.1992—
−1K984295Invacare Check O2 Plus Concentrator Analyzer (Check O2 Plus)Invacare Corp.1999—
0 (this device)K072469Digiflo Concentrator AnalyzerDigiflo, Inc.2008—
+1K112402ULTRAMAXO2 Oxygen AnalyerMaxtec, LLC2011—
+2K261389PRO2 Elite Plus Oxygen Analyzer (PRO2PLUS-1)Salter Labs2026—
+2K250002Smart Check O2 (MA0236)Life Spark Medical, LLC2025—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199910

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201110
202510
202610
FIG. 1 — Lineage of K072469, 1992–2026Source: 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 CCL? 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 CCL device

  1. #1 K261389 PRO2 Elite Plus Oxygen Analyzer (PRO2PLUS-1)score 12.7 · 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? (2)

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
*K984295Invacare Check O2 Plus Concentrator Analyzer (Check O2 Plus)
Summary page 1
…ANALYZER * Common name - DigiHH * Classification name - Oxygen gas analyzer (Product Code: CCL) Equivalence claimed to: * Invacare Check 0 lus K(984295 * PRO2 CHECK OXYGEN INDICATOR K(983500. description of the device The DigiFLO Concentrator ANALYZER is a lightweight, batt…
Invacare Corp.1999—
*K983500PRO2 Check Oxygen Indicator
Summary page 1
…* Classification name - Oxygen gas analyzer (Product Code: CCL) Equivalence claimed to: * Invacare Check 0 lus K(984295 * PRO2 CHECK OXYGEN INDICATOR K(983500. description of the device The DigiFLO Concentrator ANALYZER is a lightweight, battery operated device, which measures oxygen c…
Medical Technology Specialists, Inc.1999—

Also cleared against K984295: 1 other device →

What descends from it? (3)

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

NumberDeviceApplicantDecidedDescendants
K112402ULTRAMAXO2 Oxygen AnalyerMaxtec, LLC20112

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 16 years and passes through 3 companies; a new generation was cleared every 8.5 years on median.
  • None of the 3 ancestors has a recall.
  • Of its descendants, K112402 (Maxtec, LLC, 2011) has gone furthest, with 2 descendants of its own.
  • 1 other device also cites its predicate K984295.

How does its category compare?

All CCL devices

CCL Analyzer, Gas, Oxygen, Gaseous-Phase: FDA decisions, review times, recalls and adverse event reports over 20 years. 2008, this device’s year, is highlighted.

FDA decisions per year · CCL

2in 2025

2007: 22008: 22011: 12013: 22016: 12018: 12022: 22023: 12025: 22026 (partial year): 1
2007high 2 (2007) · low 0 (2009)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · CCL

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

Recalls per year · CCL

1in 2009

2009: 1
2007high 1 (2009) · low 0 (2007)2026

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

Adverse event reports per year · CCL

2in 2025

2007: 12008: 22009: 22010: 52011: 42012: 52013: 32014: 82015: 52016: 12017: 22018: 12019: 12020: 12021: 32023: 42024: 42025: 2
2007high 8 (2014) · low 0 (2022)2025

MAUDE reports naming product code CCL, 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
20072—01
20082—02
20090—12
20100—05
20111—04
20120—05
20132—03
20140—08
20150—05
20161—01
20170—02
20181—01
20190—01
20200—01
20210—03
20222—00
20231—04
20240—04
20252—02
20261—0—

What is it indicated for?

The DigiFLO Concentrator ANALYZER is a tool used by service personnel to measure Oxygen purity, Flow at the outlet of an oxygen concentrator. Also, it measures gas pressure inside and at the outlet of an oxygen concentrator. It is not intended to be used by patients who are prescribed oxygen, nor is it intended to continuously monitor or confirm oxygen delivery to a patient. The DigiFLO Concentrator ANALYZER is intended to be used in an environment where oxygen concentrators are being serviced or repaired. This includes Hospitals, Nursing Homes, Extended Care Facilities, Patient Homes, and Respiratory Device Service and Repair Centers.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K072469: Digiflo Concentrator Analyzer.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K072469

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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