Last synced on 14 November 2025 at 11:06 pm

PULMONE MINIBOX PFT TM

Page Type
Cleared 510(K)
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)
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