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CARDIAC EVENT RECORDER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K843533
510(k) Type
Traditional
Applicant
CRYO2 CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/28/1985
Days to Decision
294 days

CARDIAC EVENT RECORDER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K843533
510(k) Type
Traditional
Applicant
CRYO2 CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/28/1985
Days to Decision
294 days