VITAMIN B12 FOLATE CA-1515-125
K-Number: K832711 · 1983-10-04
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Device Summary
Frequently Asked Questions
What is the VITAMIN B12 FOLATE CA-1515-125?
VITAMIN B12 FOLATE CA-1515-125 is a medical device that received FDA 510(k) clearance on 1983-10-04. The listed applicant is Clinical Assays, Inc.. The 510(k) number is K832711.
When did VITAMIN B12 FOLATE CA-1515-125 receive FDA 510(k) clearance?
VITAMIN B12 FOLATE CA-1515-125 received FDA 510(k) clearance on 1983-10-04, under 510(k) number K832711.
Who is the listed applicant for VITAMIN B12 FOLATE CA-1515-125?
The FDA 510(k) record lists Clinical Assays, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VITAMIN B12 FOLATE CA-1515-125?
The FDA product code for VITAMIN B12 FOLATE CA-1515-125 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 Clinical Assays, Inc. 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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