LIQUISOL DIGOXIN RIA TEST KIT
K-Number: K780207 · 1978-02-23
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Device Summary
Frequently Asked Questions
What is the LIQUISOL DIGOXIN RIA TEST KIT?
LIQUISOL DIGOXIN RIA TEST KIT is a medical device that received FDA 510(k) clearance on 1978-02-23. The listed applicant is Damon Corp.. The 510(k) number is K780207.
When did LIQUISOL DIGOXIN RIA TEST KIT receive FDA 510(k) clearance?
LIQUISOL DIGOXIN RIA TEST KIT received FDA 510(k) clearance on 1978-02-23, under 510(k) number K780207.
Who is the listed applicant for LIQUISOL DIGOXIN RIA 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 DIGOXIN RIA TEST KIT?
The FDA product code for LIQUISOL DIGOXIN RIA TEST KIT is DON.
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: DON)
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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