Cleared Traditional

K823417 - PRISMA-C-REACTIVE PROTEIN CALIBRATORS (FDA 510(k) Clearance)

Dec 1982
Decision
24d
Days
Class 2
Risk

K823417 is an FDA 510(k) clearance for the PRISMA-C-REACTIVE PROTEIN CALIBRATORS. This device is classified as a C-reactive Protein, Antigen, Antiserum, And Control (Class II - Special Controls, product code DCK).

Submitted by Syva Co. (Mchenry, US). The FDA issued a Cleared decision on December 9, 1982, 24 days after receiving the submission on November 15, 1982.

This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 866.5270.

Submission Details

510(k) Number K823417 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 15, 1982
Decision Date December 09, 1982
Days to Decision 24 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary

Device Classification

Product Code DCK — C-reactive Protein, Antigen, Antiserum, And Control
Device Class Class II - Special Controls
CFR Regulation 21 CFR 866.5270