Liquichek Anti-Sm Control, Positive, Catalog #115

FDA 510(k) K024219 · Bio-Rad

Substantially Equivalent

510(k) numberK024219

Submission

Device name
Liquichek Anti-Sm Control, Positive, Catalog #115
Applicant
Bio-Rad
Irvine, CA, US
Received
December 23, 2002
Decision date
January 15, 2003
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
LKP – Anti-Sm Antibody, Antigen And Control
Device class
Class II (moderate risk)
Regulation
21 CFR 866.5100
Specialty
Immunology

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Questions and answers

When was Liquichek Anti-Sm Control, Positive, Catalog #115 cleared by the FDA?

Liquichek Anti-Sm Control, Positive, Catalog #115 (K024219) received a 510(k) decision of Substantially Equivalent on January 15, 2003, 23 days after the submission was received.

What is the product code of K024219?

The FDA product code is LKP – Anti-Sm Antibody, Antigen And Control, a Class II (moderate risk) device regulated under 21 CFR 866.5100.