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MODEL #350 SHOCK-PLATE DEFIB ADAPTOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K911402
510(k) Type
Traditional
Applicant
CARDIOTRONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/3/1991
Days to Decision
188 days

MODEL #350 SHOCK-PLATE DEFIB ADAPTOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K911402
510(k) Type
Traditional
Applicant
CARDIOTRONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/3/1991
Days to Decision
188 days