510(k) K920668

MINUTEX D-DIMER LATEX TEST by Biopool AB — Product Code GHH

K920668 is an FDA 510(k) premarket notification submitted by Biopool AB for the device "MINUTEX D-DIMER LATEX TEST". The FDA issued a decision of Substantially Equivalent on October 16, 1992. The device falls under product code GHH (Fibrin Split Products), a Class II device regulated under 21 CFR 864.7320. Biopool AB has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 16, 1992
Date Received
February 13, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Fibrin Split Products
Device Class
Class II
Regulation Number
864.7320
Review Panel
HE
Submission Type