Last synced on 1 July 2022 at 11:04 pm

PULMONE MINIBOX PFT TM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K133051
510(k) Type
Traditional
Applicant
PULMONE ADVANCED MEDICAL DEVICES, LTD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/2/2014
Days to Decision
217 days
Submission Type
Summary

PULMONE MINIBOX PFT TM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K133051
510(k) Type
Traditional
Applicant
PULMONE ADVANCED MEDICAL DEVICES, LTD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/2/2014
Days to Decision
217 days
Submission Type
Summary