3M N95 HOME RESPIRATOR WITH FLUID RESISTANCE— 510(k) DEN060009
Unknown3M Company
FDA 510(k) clearance DEN060009 for 3M N95 HOME RESPIRATOR WITH FLUID RESISTANCE, Unknown on 2007-05-08. Applicant: 3M Company. Device class: 2.
Clearance details
- Device name as filed
- 3M N95 HOME RESPIRATOR WITH FLUID RESISTANCE; 3M N95 HOME RESPIRATOR
- Applicant
- 3M Company
- Product code
- Code NZJ
- Device class
- Class 2
- Regulation
- 21 CFR 880.6260
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Post-NSE
- Location
- St. Paul, MN, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.