Ciba Corning Magic Lite Vitamin B12 Immunoassay

FDA 510(k) K883722 · Ciba Corning Diagnostics Corp.

Substantially Equivalent

510(k) numberK883722

Submission

Device name
Ciba Corning Magic Lite Vitamin B12 Immunoassay
Applicant
Ciba Corning Diagnostics Corp.
East Walpole, MA, US
Received
August 31, 1988
Decision date
November 4, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CDD – Radioassay, Vitamin B12
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1810
Specialty
Clinical Chemistry

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Questions and answers

When was Ciba Corning Magic Lite Vitamin B12 Immunoassay cleared by the FDA?

Ciba Corning Magic Lite Vitamin B12 Immunoassay (K883722) received a 510(k) decision of Substantially Equivalent on November 4, 1988, 65 days after the submission was received.

What is the product code of K883722?

The FDA product code is CDD – Radioassay, Vitamin B12, a Class II (moderate risk) device regulated under 21 CFR 862.1810.