510(k) K981871

C-REACTIVE PROTEIN ELISA, MODEL NUMBER DSL-10-42100 by Diagnostic Systems Laboratories, Inc. — Product Code DCK

K981871 is an FDA 510(k) premarket notification submitted by Diagnostic Systems Laboratories, Inc. for the device "C-REACTIVE PROTEIN ELISA, MODEL NUMBER DSL-10-42100". The FDA issued a decision of Substantially Equivalent on November 9, 1998. The device falls under product code DCK (C-Reactive Protein, Antigen, Antiserum, And Control), a Class II device regulated under 21 CFR 866.5270. Diagnostic Systems Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 9, 1998
Date Received
May 28, 1998
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
C-Reactive Protein, Antigen, Antiserum, And Control
Device Class
Class II
Regulation Number
866.5270
Review Panel
IM
Submission Type