Last synced on 25 January 2026 at 3:41 am

AMCO REPLACEMENT BATTERY FOR POWERHEART AED, NON-RECHARGEABLE, MODEL 2L561; G3, NON-RECHARGABLE, MODEL 7L561

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082861
510(k) Type
Traditional
Applicant
Amco International Manufacturing & Design, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/25/2008
Days to Decision
57 days
Submission Type
Summary

AMCO REPLACEMENT BATTERY FOR POWERHEART AED, NON-RECHARGEABLE, MODEL 2L561; G3, NON-RECHARGABLE, MODEL 7L561

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082861
510(k) Type
Traditional
Applicant
Amco International Manufacturing & Design, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/25/2008
Days to Decision
57 days
Submission Type
Summary