Last synced on 24 June 2022 at 11:05 pm

AERONEB PRO

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K120939
510(k) Type
Special
Applicant
AEROGEN LTD
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
4/26/2012
Days to Decision
28 days
Submission Type
Statement

AERONEB PRO

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K120939
510(k) Type
Special
Applicant
AEROGEN LTD
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
4/26/2012
Days to Decision
28 days
Submission Type
Statement