RABBIT ANTISERUM TO HUMAN KAPPA LIGHT
K-Number: K831904 · 1983-07-19
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Device Summary
Frequently Asked Questions
What is the RABBIT ANTISERUM TO HUMAN KAPPA LIGHT?
RABBIT ANTISERUM TO HUMAN KAPPA LIGHT is a medical device that received FDA 510(k) clearance on 1983-07-19. The listed applicant is Dako Corp.. The 510(k) number is K831904.
When did RABBIT ANTISERUM TO HUMAN KAPPA LIGHT receive FDA 510(k) clearance?
RABBIT ANTISERUM TO HUMAN KAPPA LIGHT received FDA 510(k) clearance on 1983-07-19, under 510(k) number K831904.
Who is the listed applicant for RABBIT ANTISERUM TO HUMAN KAPPA LIGHT?
The FDA 510(k) record lists Dako Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RABBIT ANTISERUM TO HUMAN KAPPA LIGHT?
The FDA product code for RABBIT ANTISERUM TO HUMAN KAPPA LIGHT is DEO.
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 Dako 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: DEO)
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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