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NGDI (NEXT GENERATION DIAGNOSTIC INSTRUMENT)

Page Type
Cleared 510(K)
510(k) Number
K040913
510(k) Type
Traditional
Applicant
BAUSCH & LOMB
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/23/2004
Days to Decision
106 days
Submission Type
Summary

NGDI (NEXT GENERATION DIAGNOSTIC INSTRUMENT)

Page Type
Cleared 510(K)
510(k) Number
K040913
510(k) Type
Traditional
Applicant
BAUSCH & LOMB
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/23/2004
Days to Decision
106 days
Submission Type
Summary