Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

VITAMIN B12 57CO/FOLATE 125I -

K-Number: K840462 · 1984-06-25

Decision Date1984-06-25
Product CodeCDD
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

VITAMIN B12 57CO/FOLATE 125I - is the device name listed in this FDA 510(k) record. The listed applicant is Corning Medical & Scientific. It received FDA 510(k) clearance on 1984-06-25 under 510(k) number K840462. The device is classified under product code CDD. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 111 devices →

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.

↑