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FDA 510(k) Application Details - K231711
Device Classification Name
Test, Time, Prothrombin
More FDA Info for this Device
510(K) Number
K231711
Device Name
Test, Time, Prothrombin
Applicant
iLine Microsystems S.L.
Paseo Mikeletegi, 69
San Sebastian-Donostia 20009 ES
Other 510(k) Applications for this Company
Contact
Miren Itsaso Hormaeche
Other 510(k) Applications for this Contact
Regulation Number
864.7750
More FDA Info for this Regulation Number
Classification Product Code
GJS
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
06/12/2023
Decision Date
07/11/2023
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
HE - Hematology
Review Advisory Committee
HE - Hematology
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
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