510(k) K915163

PROTEIN S EID KIT AND PROTEIN S EID BULK PLATES by Biopool AB — Product Code GGP

K915163 is an FDA 510(k) premarket notification submitted by Biopool AB for the device "PROTEIN S EID KIT AND PROTEIN S EID BULK PLATES". The FDA issued a decision of Substantially Equivalent on January 6, 1992. The device falls under product code GGP (Test, Qualitative And Quantitative Factor Deficiency), a Class II device regulated under 21 CFR 864.7290. Biopool AB has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 6, 1992
Date Received
November 14, 1991
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Test, Qualitative And Quantitative Factor Deficiency
Device Class
Class II
Regulation Number
864.7290
Review Panel
HE
Submission Type