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LUMAPROBE

Page Type
Cleared 510(K)
510(k) Number
K073000
510(k) Type
Traditional
Applicant
CLAREBLEND, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/1/2008
Days to Decision
343 days
Submission Type
Summary

LUMAPROBE

Page Type
Cleared 510(K)
510(k) Number
K073000
510(k) Type
Traditional
Applicant
CLAREBLEND, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/1/2008
Days to Decision
343 days
Submission Type
Summary