CIBA CORNING MAGIC LITE VITAMIN B12 IMMUNOASSAY
K-Number: K883722 · 1988-11-04
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Device Summary
Frequently Asked Questions
What is the CIBA CORNING MAGIC LITE VITAMIN B12 IMMUNOASSAY?
CIBA CORNING MAGIC LITE VITAMIN B12 IMMUNOASSAY is a medical device that received FDA 510(k) clearance on 1988-11-04. The listed applicant is Ciba Corning Diagnostics Corp.. The 510(k) number is K883722.
When did CIBA CORNING MAGIC LITE VITAMIN B12 IMMUNOASSAY receive FDA 510(k) clearance?
CIBA CORNING MAGIC LITE VITAMIN B12 IMMUNOASSAY received FDA 510(k) clearance on 1988-11-04, under 510(k) number K883722.
Who is the listed applicant for CIBA CORNING MAGIC LITE VITAMIN B12 IMMUNOASSAY?
The FDA 510(k) record lists Ciba Corning Diagnostics Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CIBA CORNING MAGIC LITE VITAMIN B12 IMMUNOASSAY?
The FDA product code for CIBA CORNING MAGIC LITE VITAMIN B12 IMMUNOASSAY is CDD.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Ciba Corning Diagnostics Corp. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: CDD)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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