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BRIDGE III RECEIVER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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