510(k) K873726

ACID PHOSPHATASE TEST by King Diagnostics, Inc. — Product Code CKE

K873726 is an FDA 510(k) premarket notification submitted by King Diagnostics, Inc. for the device "ACID PHOSPHATASE TEST". The FDA issued a decision of Substantially Equivalent on January 27, 1988. The device falls under product code CKE (Acid Phosphatase, Thymolphthale Inmonophosphate), a Class II device regulated under 21 CFR 862.1020. King Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 27, 1988
Date Received
September 15, 1987
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