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CARDIOBEEPER CB250

Page Type
Cleared 510(K)
510(k) Number
K983582
510(k) Type
Traditional
Applicant
MERDIAN MEDICAL TECHNOLOGIES LTD.
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
11/13/1998
Days to Decision
31 days
Submission Type
Summary

CARDIOBEEPER CB250

Page Type
Cleared 510(K)
510(k) Number
K983582
510(k) Type
Traditional
Applicant
MERDIAN MEDICAL TECHNOLOGIES LTD.
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
11/13/1998
Days to Decision
31 days
Submission Type
Summary