510(k) K992711

SIGMA DIAGNOSTICS ALEXIN HS, MODELS A0969, A1094 by Sigma Diagnostics, Inc. — Product Code GFO

K992711 is an FDA 510(k) premarket notification submitted by Sigma Diagnostics, Inc. for the device "SIGMA DIAGNOSTICS ALEXIN HS, MODELS A0969, A1094". The FDA issued a decision of Substantially Equivalent on December 6, 1999. The device falls under product code GFO (Activated 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
December 6, 1999
Date Received
August 11, 1999
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Activated Partial Thromboplastin
Device Class
Class II
Regulation Number
864.7925
Review Panel
HE
Submission Type