BUNN VOLUMAIRE RESPIRATORY EXERCISER— 510(k) K800546
Substantially EquivalentThe John Bunn Co.
FDA 510(k) clearance K800546 for BUNN VOLUMAIRE RESPIRATORY EXERCISER, Substantially Equivalent on 1980-03-25. Applicant: The John Bunn Co.. Device class: 2.
Clearance details
- Applicant
- The John Bunn Co.
- Product code
- Code BWF
- Device class
- Class 2
- Regulation
- 21 CFR 868.5690
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Recent devices under product code BWF
view allMore clearances from The John Bunn Co.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.