Quantimetric 2 C-Reactive Protein Reag.

FDA 510(k) K821984 · Kallestad Laboratories, Inc.

Substantially Equivalent

510(k) numberK821984

Submission

Device name
Quantimetric 2 C-Reactive Protein Reag.
Applicant
Kallestad Laboratories, Inc.
Mchenry, IL, US
Received
July 6, 1982
Decision date
July 22, 1982
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DCK – C-Reactive Protein, Antigen, Antiserum, And Control
Device class
Class II (moderate risk)
Regulation
21 CFR 866.5270
Specialty
Immunology

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Questions and answers

When was Quantimetric 2 C-Reactive Protein Reag. cleared by the FDA?

Quantimetric 2 C-Reactive Protein Reag. (K821984) received a 510(k) decision of Substantially Equivalent on July 22, 1982, 16 days after the submission was received.

What is the product code of K821984?

The FDA product code is DCK – C-Reactive Protein, Antigen, Antiserum, And Control, a Class II (moderate risk) device regulated under 21 CFR 866.5270.