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CARDIACMONITOR

Page Type
Cleared 510(K)
510(k) Number
K963375
510(k) Type
Traditional
Applicant
VISION ELECTRONICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/28/1997
Days to Decision
185 days
Submission Type
Summary

CARDIACMONITOR

Page Type
Cleared 510(K)
510(k) Number
K963375
510(k) Type
Traditional
Applicant
VISION ELECTRONICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/28/1997
Days to Decision
185 days
Submission Type
Summary