DIAGNON B12 57CO RIA KIT
K-Number: K832717 · 1983-12-08
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Device Summary
Frequently Asked Questions
What is the DIAGNON B12 57CO RIA KIT?
DIAGNON B12 57CO RIA KIT is a medical device that received FDA 510(k) clearance on 1983-12-08. The listed applicant is Diagnon Corp.. The 510(k) number is K832717.
When did DIAGNON B12 57CO RIA KIT receive FDA 510(k) clearance?
DIAGNON B12 57CO RIA KIT received FDA 510(k) clearance on 1983-12-08, under 510(k) number K832717.
Who is the listed applicant for DIAGNON B12 57CO RIA KIT?
The FDA 510(k) record lists Diagnon Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DIAGNON B12 57CO RIA KIT?
The FDA product code for DIAGNON B12 57CO RIA KIT 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 Diagnon Corp. 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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