510(k) Report

510(k) · Cleared

Cleared

Pollenex Hepa Air Cleaners

K925055510(k) TraditionalCleared May 18, 1994589-day reviewClass II21 CFR 880.5045

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

Pollenex Corp. · FRF Cleaner, Air, Medical Recirculating

Cleared on May 18, 1994 after a 589-day review. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

Decided
May 18, 1994
Review
589 days
Class
Class II
Product code
FRF
Recalls
None
Predicates
0

FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

FIG. 1 — Lineage of K925055Source: FDA 510(k) database · How lineage is built

Get the monthly Device Review Tracker

Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in FRF? 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 FRF device

  1. #1 K200321 Novaerus NV1050score 9.9 · 2 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?

FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

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.

How does its category compare?

All FRF devices

FRF Cleaner, Air, Medical Recirculating: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · FRF

1in 2025

2007: 12008: 22013: 22020: 12022: 32023: 22024: 22025: 1
2007high 3 (2022) · low 0 (2009)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FRF

163in 2022

2022: 163 days median
2007high 163 (2022)2026

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

Recalls per year · FRF

1in 2012

2012: 1
2007high 1 (2012) · low 0 (2007)2026

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

Adverse event reports per year · FRF

3in 2013

2007: 22008: 32011: 12012: 32013: 3
2007high 3 (2008) · low 0 (2009)2025

MAUDE reports naming product code FRF, 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—02
20082—03
20090—00
20100—00
20110—01
20120—13
20132—03
20140—00
20150—00
20160—00
20170—00
20180—00
20190—00
20201—00
20210—00
2022316300
20232—00
20242—00
20251—00
20260—0—
Cite this page

510(k) Report. “K925055: Pollenex Hepa Air Cleaners.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K925055

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

Record history
  • FDA decision record loaded May 2, 2026
  • Page last updated Nov 3, 2026