CORNING VITAMIN B12 FOLATE DEFIC. CONTR.
K-Number: K810952 · 1981-04-17
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Device Summary
Frequently Asked Questions
What is the CORNING VITAMIN B12 FOLATE DEFIC. CONTR.?
CORNING VITAMIN B12 FOLATE DEFIC. CONTR. is a medical device that received FDA 510(k) clearance on 1981-04-17. The listed applicant is Corning Medical & Scientific. The 510(k) number is K810952.
When did CORNING VITAMIN B12 FOLATE DEFIC. CONTR. receive FDA 510(k) clearance?
CORNING VITAMIN B12 FOLATE DEFIC. CONTR. received FDA 510(k) clearance on 1981-04-17, under 510(k) number K810952.
Who is the listed applicant for CORNING VITAMIN B12 FOLATE DEFIC. CONTR.?
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 CORNING VITAMIN B12 FOLATE DEFIC. CONTR.?
The FDA product code for CORNING VITAMIN B12 FOLATE DEFIC. CONTR. is JJY.
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: JJY)
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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