VITAMIN B12 57CO/FOLATE 125I -
K-Number: K840462 · 1984-06-25
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Device Summary
Frequently Asked Questions
What is the VITAMIN B12 57CO/FOLATE 125I -?
VITAMIN B12 57CO/FOLATE 125I - is a medical device that received FDA 510(k) clearance on 1984-06-25. The listed applicant is Corning Medical & Scientific. The 510(k) number is K840462.
When did VITAMIN B12 57CO/FOLATE 125I - receive FDA 510(k) clearance?
VITAMIN B12 57CO/FOLATE 125I - received FDA 510(k) clearance on 1984-06-25, under 510(k) number K840462.
Who is the listed applicant for VITAMIN B12 57CO/FOLATE 125I -?
The FDA 510(k) record lists Corning Medical & Scientific as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VITAMIN B12 57CO/FOLATE 125I -?
The FDA product code for VITAMIN B12 57CO/FOLATE 125I - 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 Corning Medical & Scientific 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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