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IKONISCOPE ONCOFISH BLADDER TEST SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K062755
510(k) Type
Traditional
Applicant
Ikonisys, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/4/2007
Days to Decision
112 days
Submission Type
Summary

IKONISCOPE ONCOFISH BLADDER TEST SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K062755
510(k) Type
Traditional
Applicant
Ikonisys, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/4/2007
Days to Decision
112 days
Submission Type
Summary