Last synced on 23 February 2024 at 11:04 pm

ACTIHEART

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K052489
510(k) Type
Traditional
Applicant
RESPIRONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/27/2005
Days to Decision
15 days
Submission Type
Summary

ACTIHEART

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K052489
510(k) Type
Traditional
Applicant
RESPIRONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/27/2005
Days to Decision
15 days
Submission Type
Summary