510(k) K972116

VON WILLEBRAND REAGENT by Behring Diagnostics, Inc. — Product Code GGP

K972116 is an FDA 510(k) premarket notification submitted by Behring Diagnostics, Inc. for the device "VON WILLEBRAND REAGENT". The FDA issued a decision of Substantially Equivalent on July 25, 1997. The device falls under product code GGP (Test, Qualitative And Quantitative Factor Deficiency), a Class II device regulated under 21 CFR 864.7290. Behring Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 25, 1997
Date Received
June 5, 1997
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