Last synced on 14 November 2025 at 11:06 pm

IKONISCOPE FASTFISH AUTO/AMNIOCYTE TEST SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K061392
510(k) Type
Traditional
Applicant
Ikonisys, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/2006
Days to Decision
74 days
Submission Type
Summary

IKONISCOPE FASTFISH AUTO/AMNIOCYTE TEST SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K061392
510(k) Type
Traditional
Applicant
Ikonisys, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/2006
Days to Decision
74 days
Submission Type
Summary