510(k) K823453

VON WILLEBRAND FACTOR ASSAY by General Diagnostics — Product Code GGP

K823453 is an FDA 510(k) premarket notification submitted by General Diagnostics for the device "VON WILLEBRAND FACTOR ASSAY". The FDA issued a decision of Substantially Equivalent on January 21, 1983. The device falls under product code GGP (Test, Qualitative And Quantitative Factor Deficiency), a Class II device regulated under 21 CFR 864.7290. General Diagnostics has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 21, 1983
Date Received
November 17, 1982
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