Atlas FDA

Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Porous Media Corp. · Predicate Candidate Screening

9 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

88 daysmedian FDA review time
405 days90th percentile
9clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K062091POROUS MEDIA HUMIDIFLOW HUMIDIFIER FOR UNIVERSAL HUMIDIFICATPorous Media Corp.2006-08-08151
K061426OXYGEN CONCENTRATOR FILTERS, MODELS DBF32, DBF24, DBF27, DBFPorous Media Corp.2006-06-05130
K990276POROUS MEDIA DPB30 SERIES DISPOSABLE PRE-BYPASS FILTERPorous Media Corp.1999-10-012460
K982385POROUS MEDIA DPB20 SERIES DISPOSABLE PRE-BYPASS FILTERPorous Media Corp.1999-02-012070
K982127POROUS MEDIA DEF25 DISPOSABLE RESPIRATORY FILTERPorous Media Corp.1998-06-2360
K965020POROUS MEDIA DBF23 REUSABLE RESPIRATORY FILTERPorous Media Corp.1997-03-14880
K964979POROUS MEDIA DBF23 DISPOSABLE RESPIRATORY FILTERPorous Media Corp.1997-03-11890
K952428POROUS MEDIA DBF23-R REUSABLE RESPIRATORY FILTERPorous Media Corp.1995-07-07440
K934132POROUS MEDIA DBF23 DISPOSABLE RESPIRATORY FILTERPorous Media Corp.1994-10-044050

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams: atlasbyauro.com/fda