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BRIDGE III RECEIVER

Page Type
Cleared 510(K)
510(k) Number
K010794
510(k) Type
Traditional
Applicant
MERIDIAN MEDICAL TECHNOLOGIES LTD.
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
5/10/2001
Days to Decision
55 days
Submission Type
Summary

BRIDGE III RECEIVER

Page Type
Cleared 510(K)
510(k) Number
K010794
510(k) Type
Traditional
Applicant
MERIDIAN MEDICAL TECHNOLOGIES LTD.
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
5/10/2001
Days to Decision
55 days
Submission Type
Summary