510(k) K915463

ACTIVATED PARTIAL THROMBOPLASTIN TIME by Sigma Diagnostics, Inc. — Product Code GGW

K915463 is an FDA 510(k) premarket notification submitted by Sigma Diagnostics, Inc. for the device "ACTIVATED PARTIAL THROMBOPLASTIN TIME". The FDA issued a decision of Substantially Equivalent on January 23, 1992. The device falls under product code GGW (Test, Time, Partial Thromboplastin), a Class II device regulated under 21 CFR 864.7925. Sigma Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 23, 1992
Date Received
December 4, 1991
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Test, Time, Partial Thromboplastin
Device Class
Class II
Regulation Number
864.7925
Review Panel
HE
Submission Type