EB-VCA, TEST, ANTIBODY, FLUORESCENT
K-Number: K780925 · 1978-06-22
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Device Summary
Frequently Asked Questions
What is the EB-VCA, TEST, ANTIBODY, FLUORESCENT?
EB-VCA, TEST, ANTIBODY, FLUORESCENT is a medical device that received FDA 510(k) clearance on 1978-06-22. The listed applicant is Litton Bionetics. The 510(k) number is K780925.
When did EB-VCA, TEST, ANTIBODY, FLUORESCENT receive FDA 510(k) clearance?
EB-VCA, TEST, ANTIBODY, FLUORESCENT received FDA 510(k) clearance on 1978-06-22, under 510(k) number K780925.
Who is the listed applicant for EB-VCA, TEST, ANTIBODY, FLUORESCENT?
The FDA 510(k) record lists Litton Bionetics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EB-VCA, TEST, ANTIBODY, FLUORESCENT?
The FDA product code for EB-VCA, TEST, ANTIBODY, FLUORESCENT is JRY.
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 Litton Bionetics 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: JRY)
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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