LIQUISOL TESTOSTERONE RADIOIMM. TEST KIT
K-Number: K802661 · 1980-12-10
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Device Summary
Frequently Asked Questions
What is the LIQUISOL TESTOSTERONE RADIOIMM. TEST KIT?
LIQUISOL TESTOSTERONE RADIOIMM. TEST KIT is a medical device that received FDA 510(k) clearance on 1980-12-10. The listed applicant is Damon Corp.. The 510(k) number is K802661.
When did LIQUISOL TESTOSTERONE RADIOIMM. TEST KIT receive FDA 510(k) clearance?
LIQUISOL TESTOSTERONE RADIOIMM. TEST KIT received FDA 510(k) clearance on 1980-12-10, under 510(k) number K802661.
Who is the listed applicant for LIQUISOL TESTOSTERONE RADIOIMM. TEST KIT?
The FDA 510(k) record lists Damon Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LIQUISOL TESTOSTERONE RADIOIMM. TEST KIT?
The FDA product code for LIQUISOL TESTOSTERONE RADIOIMM. TEST KIT is CDZ.
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 Damon 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: CDZ)
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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