510(k) · Cleared
ClearedPurgo
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Aeroclean Technologies, LLC · FRA Purifier, Air, Ultraviolet, Medical
Cleared on Jun 1, 2022 as substantially equivalent to K211194 (Molekule, Inc., 2021) and 1 other predicate after a 183-day review. Its family tree reaches back 7 generations to 2003. 1 later device descends from it.
- Decided
- Jun 1, 2022
- Review
- 183 days
- Class
- Class II
- Product code
- FRA
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 7 generations to K023830 (2003). 1 later device descends from it, 1 citing it directly.
- Root · 7 generations backK023830 Airocide TI02Kes Science & Technology, Inc. · 2003
- 6 generations backK033448 Electro-Optical Air Sterilizer with IonizerJohn Mfg., Ltd. · 2004
- 5 generations backK052732 Abracair Air Cleaner, Model QTZ300-60; Abracair Air Cleaner, Model…Abracair, Inc. · 2006
- 4 generations backK161468 Transformair Indoor Air PurifierTransformair, LLC · 2017
- 3 generations backK200500 Molekule Air Pro RXMolekule, Inc. · 2020
- 2 generations backK202339 Molekule Air Mini, Molekule Air Mini +Molekule, Inc. · 2021
- 1 generation backK211194 Molekule Air ProMolekule, Inc. · 2021
- This deviceK213753 PurgoAeroclean Technologies, LLC · 2022
- Descendant · cites it directly · 0 of its ownK223328 PurgoAeroclean Technologies, Inc. · 2022
Most influential descendants
Showing 1 of 1 · See all- K223328PurgoAeroclean Technologies, Inc. · 2022 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −7 | K023830 | Airocide TI02 | Kes Science & Technology, Inc. | 2003 | — |
| −6 | K033448 | Electro-Optical Air Sterilizer with Ionizer | John Mfg., Ltd. | 2004 | — |
| −5 | K052732 | Abracair Air Cleaner, Model QTZ300-60; Abracair Air Cleaner, Model TI 100-30P | Abracair, Inc. | 2006 | — |
| −4 | K161468 | Transformair Indoor Air Purifier | Transformair, LLC | 2017 | — |
| −3 | K200500 | Molekule Air Pro RX | Molekule, Inc. | 2020 | — |
| −2 | K202339 | Molekule Air Mini, Molekule Air Mini + | Molekule, Inc. | 2021 | — |
| −1 | K211194 | Molekule Air Pro | Molekule, Inc. | 2021 | — |
| 0 (this device) | K213753 | Purgo | Aeroclean Technologies, LLC | 2022 | — |
| +1 | K223328 | Purgo | Aeroclean Technologies, Inc. | 2022 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2022 | 1 | 0 |
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 FRA? 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 FRA device
- #1 K212644 Aura Stormscore 13.9 · 6 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K211194 | Molekule Air ProSummary page 4…Molekule Air Pro Molekule Air Pro RX 510(k) Submitter / Holder Molekule, Inc. Molekule, Inc. 510(k) Number K211194 K200500 Regulation Number 21 CFR 880.6500 21 CFR 880.6500 Classific… | 2021 |
| * | K200500 | Molekule Air Pro RXSummary page 4…Molekule Air Pro RX 510(k) Submitter / Holder Molekule, Inc. Molekule, Inc. 510(k) Number K211194 K200500 Regulation Number 21 CFR 880.6500 21 CFR 880.6500 Classification Class II… | 2020 |
What descends from it? (1)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K223328 | Purgo | 2022 | 0 |
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 19 years and passes through 6 companies; a new generation was cleared every 1.4 years on median.
- None of the 7 ancestors has a recall.
- Of its descendants, K223328 (Aeroclean Technologies, Inc., 2022) has gone furthest, with 0 descendants of its own.
- 1 other device also cites its predicate K211194.
How does its category compare?
All FRA devicesFRA Purifier, Air, Ultraviolet, Medical: FDA decisions, review times, recalls and adverse event reports over 20 years. 2022, this device’s year, is highlighted.
FDA decisions per year · FRA
1in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · FRA
205in 2024
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · FRA
No recall names FRA since 2007.
Adverse event reports per year · FRA
2in 2024
MAUDE reports naming product code FRA, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 0 | — | 0 | 0 |
| 2008 | 0 | — | 0 | 0 |
| 2009 | 0 | — | 0 | 0 |
| 2010 | 0 | — | 0 | 0 |
| 2011 | 0 | — | 0 | 0 |
| 2012 | 0 | — | 0 | 0 |
| 2013 | 0 | — | 0 | 0 |
| 2014 | 1 | — | 0 | 0 |
| 2015 | 0 | — | 0 | 1 |
| 2016 | 0 | — | 0 | 0 |
| 2017 | 1 | — | 0 | 0 |
| 2018 | 0 | — | 0 | 0 |
| 2019 | 0 | — | 0 | 0 |
| 2020 | 2 | — | 0 | 0 |
| 2021 | 5 | 190 | 0 | 1 |
| 2022 | 4 | 175 | 0 | 1 |
| 2023 | 2 | — | 0 | 0 |
| 2024 | 4 | 205 | 0 | 2 |
| 2025 | 1 | — | 0 | 0 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
Pūrgo is a combination UV and air filtration device, equipped with UV-C LEDs and a True HEPA filter intended for the reduction of bacteria, virus, fungal spores, and particles in air for use in medical facilities and other indoor spaces. Pūrgo is non-sterile.
Pūrgo has been demonstrated to remove the following organisms under the following exposure conditions:
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K213753 · printed Nov 6, 2026
Cite this page
510(k) Report. “K213753: Purgo.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K213753
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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