510(k) K961892

SPECKTIN-LA TEST SET by Analytical Control Systems, Inc. — Product Code GFO

K961892 is an FDA 510(k) premarket notification submitted by Analytical Control Systems, Inc. for the device "SPECKTIN-LA TEST SET". The FDA issued a decision of Substantially Equivalent on March 7, 1997. The device falls under product code GFO (Activated Partial Thromboplastin), a Class II device regulated under 21 CFR 864.7925. Analytical Control Systems, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 7, 1997
Date Received
May 16, 1996
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