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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
K021340
510(k) Type
Traditional
Applicant
External Counterpulsation Lab
Country
China
FDA Decision
Substantially Equivalent
Decision Date
1/30/2003
Days to Decision
279 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
K021340
510(k) Type
Traditional
Applicant
External Counterpulsation Lab
Country
China
FDA Decision
Substantially Equivalent
Decision Date
1/30/2003
Days to Decision
279 days
Submission Type
Statement