POROUS MEDIA DBF23 REUSABLE RESPIRATORY FILTER— 510(k) K965020
Substantially EquivalentPorous Media Corp.
FDA 510(k) clearance K965020 for POROUS MEDIA DBF23 REUSABLE RESPIRATORY FILTER, Substantially Equivalent on 1997-03-14. Applicant: Porous Media Corp.. Device class: 2.
Clearance details
- Applicant
- Porous Media Corp.
- Product code
- Code CAH
- Device class
- Class 2
- Regulation
- 21 CFR 868.5260
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- St. Paul, MN, US
Recent devices under product code CAH
view allMore clearances from Porous Media Corp.
view all- K062091 — POROUS MEDIA HUMIDIFLOW HUMIDIFIER FOR UNIVERSAL HUMIDIFICATION
- K061426 — OXYGEN CONCENTRATOR FILTERS, MODELS DBF32, DBF24, DBF27, DBF25, DFC06 AND DDF47
- K990276 — POROUS MEDIA DPB30 SERIES DISPOSABLE PRE-BYPASS FILTER
- K982385 — POROUS MEDIA DPB20 SERIES DISPOSABLE PRE-BYPASS FILTER
- K982127 — POROUS MEDIA DEF25 DISPOSABLE RESPIRATORY FILTER
Adverse events under product code CAH
product code CAH- Death
- 7
- Total
- 7
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.