510(k) K860476

ACID PHOSPHATASE REAGENT SET by Sterling Diagnostics, Inc. — Product Code CKE

K860476 is an FDA 510(k) premarket notification submitted by Sterling Diagnostics, Inc. for the device "ACID PHOSPHATASE REAGENT SET". The FDA issued a decision of Substantially Equivalent on March 5, 1986. The device falls under product code CKE (Acid Phosphatase, Thymolphthale Inmonophosphate), a Class II device regulated under 21 CFR 862.1020. Sterling Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 5, 1986
Date Received
February 7, 1986
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Acid Phosphatase, Thymolphthale Inmonophosphate
Device Class
Class II
Regulation Number
862.1020
Review Panel
CH
Submission Type