RIANEN, VITAMIN B12 ASSAY SYSTEM
K-Number: K792175 · 1979-11-13
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Device Summary
Frequently Asked Questions
What is the RIANEN, VITAMIN B12 ASSAY SYSTEM?
RIANEN, VITAMIN B12 ASSAY SYSTEM is a medical device that received FDA 510(k) clearance on 1979-11-13. The listed applicant is New England Nuclear. The 510(k) number is K792175.
When did RIANEN, VITAMIN B12 ASSAY SYSTEM receive FDA 510(k) clearance?
RIANEN, VITAMIN B12 ASSAY SYSTEM received FDA 510(k) clearance on 1979-11-13, under 510(k) number K792175.
Who is the listed applicant for RIANEN, VITAMIN B12 ASSAY SYSTEM?
The FDA 510(k) record lists New England Nuclear as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RIANEN, VITAMIN B12 ASSAY SYSTEM?
The FDA product code for RIANEN, VITAMIN B12 ASSAY SYSTEM 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 New England Nuclear 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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