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CRYSTAL MONITOR MODEL 16

Page Type
Cleared 510(K)
510(k) Number
K013863
510(k) Type
Traditional
Applicant
CLEVELAND MEDICAL DEVICES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/19/2002
Days to Decision
90 days
Submission Type
Summary

CRYSTAL MONITOR MODEL 16

Page Type
Cleared 510(K)
510(k) Number
K013863
510(k) Type
Traditional
Applicant
CLEVELAND MEDICAL DEVICES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/19/2002
Days to Decision
90 days
Submission Type
Summary