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MONITOR, PATIENT, MODEL PM-I0N

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K770968
510(k) Type
Traditional
Applicant
CAVITRON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/8/1977
Days to Decision
8 days

MONITOR, PATIENT, MODEL PM-I0N

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K770968
510(k) Type
Traditional
Applicant
CAVITRON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/8/1977
Days to Decision
8 days