ARTIFICIAL K-NOSE BREATHAID— 510(k) K771431
Substantially EquivalentTerumo America, Inc.
FDA 510(k) clearance K771431 for ARTIFICIAL K-NOSE BREATHAID, Substantially Equivalent on 1977-09-28. Applicant: Terumo America, Inc..
Clearance details
- Applicant
- Terumo America, Inc.
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.