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CARDIOSONIC ACOUSTIC AMPLIFIER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K813510
510(k) Type
Traditional
Applicant
SRS CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/12/1982
Days to Decision
28 days

CARDIOSONIC ACOUSTIC AMPLIFIER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K813510
510(k) Type
Traditional
Applicant
SRS CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/12/1982
Days to Decision
28 days