510(k) K896092

ALKALINE PHOSPHATASE, LEUKOCYTE, KIT by Sigma Chemical Co. — Product Code GHD

K896092 is an FDA 510(k) premarket notification submitted by Sigma Chemical Co. for the device "ALKALINE PHOSPHATASE, LEUKOCYTE, KIT". The FDA issued a decision of Substantially Equivalent on November 9, 1989. The device falls under product code GHD (Test, Leukocyte Alkaline Phosphatase), a Class I device regulated under 21 CFR 864.7660. Sigma Chemical Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 9, 1989
Date Received
October 19, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Test, Leukocyte Alkaline Phosphatase
Device Class
Class I
Regulation Number
864.7660
Review Panel
HE
Submission Type