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AECP-A, AUTOMATIC EXTERNAL COUNTERPULSATION DEVICE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012141
510(k) Type
Traditional
Applicant
External Counterpulsation Lab
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
10/25/2001
Days to Decision
107 days
Submission Type
Statement

AECP-A, AUTOMATIC EXTERNAL COUNTERPULSATION DEVICE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012141
510(k) Type
Traditional
Applicant
External Counterpulsation Lab
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
10/25/2001
Days to Decision
107 days
Submission Type
Statement