510(k) K980885

SHIELD ACTIVATED FACTOR XII (ELISA) ASSAY by Shield Diagnostics, Ltd. — Product Code GGP

K980885 is an FDA 510(k) premarket notification submitted by Shield Diagnostics, Ltd. for the device "SHIELD ACTIVATED FACTOR XII (ELISA) ASSAY". The FDA issued a decision of Substantially Equivalent on August 21, 1998. The device falls under product code GGP (Test, Qualitative And Quantitative Factor Deficiency), a Class II device regulated under 21 CFR 864.7290. Shield Diagnostics, Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 21, 1998
Date Received
March 9, 1998
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