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PULMODYNE CHF FLOW GENERATOR SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K080256
510(k) Type
Traditional
Applicant
PULMODYNE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/2008
Days to Decision
99 days
Submission Type
Summary

PULMODYNE CHF FLOW GENERATOR SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K080256
510(k) Type
Traditional
Applicant
PULMODYNE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/2008
Days to Decision
99 days
Submission Type
Summary