CORNING'S MAGIC T3(125I) RADIOIMMUNO-
K-Number: K832353 · 1983-08-31
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Device Summary
Frequently Asked Questions
What is the CORNING'S MAGIC T3(125I) RADIOIMMUNO-?
CORNING'S MAGIC T3(125I) RADIOIMMUNO- is a medical device that received FDA 510(k) clearance on 1983-08-31. The listed applicant is Corning Medical & Scientific. The 510(k) number is K832353.
When did CORNING'S MAGIC T3(125I) RADIOIMMUNO- receive FDA 510(k) clearance?
CORNING'S MAGIC T3(125I) RADIOIMMUNO- received FDA 510(k) clearance on 1983-08-31, under 510(k) number K832353.
Who is the listed applicant for CORNING'S MAGIC T3(125I) RADIOIMMUNO-?
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'S MAGIC T3(125I) RADIOIMMUNO-?
The FDA product code for CORNING'S MAGIC T3(125I) RADIOIMMUNO- is CDP.
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: CDP)
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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