510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K965020Substantially Equivalent

Porous Media Dbf23 Reusable Respiratory Filter

Pentair Filtration Solutions, St. Paul MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K965020 is the FDA 510(k) clearance record for POROUS MEDIA DBF23 REUSABLE RESPIRATORY FILTER, a class II device, cleared for Porous Media Corp. on under FDA product code CAH (Filter, Bacterial, Breathing-Circuit). FDA records list 9 510(k) clearances for Pentair Filtration Solutions, from to . As of , FDA records show no recalls naming K965020.

Clearance record

Decision date
Received
(88 days to decision)
Product code
CAH Filter, Bacterial, Breathing-Circuit
Regulation
21 CFR 868.5260
Device class
Class II
Review panel
Anesthesiology
Applicant
Porous Media Corp. 1350 Hammond Rd., St. Paul MN
510(k) summary
Statement
Third party review
No

Clearances, product code CAH

Trailing 12 months
2 clearances under product code CAH in the twelve months to October 2026, April 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code CAH, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20261
May 20261
June 20260
July 20260
August 20260
September 20260
October 20260