ELVI 444 BILITRON
K-Number: K840757 · 1984-05-30
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Device Summary
Frequently Asked Questions
What is the ELVI 444 BILITRON?
ELVI 444 BILITRON is a medical device that received FDA 510(k) clearance on 1984-05-30. The listed applicant is Logos Scientific, Inc.. The 510(k) number is K840757.
When did ELVI 444 BILITRON receive FDA 510(k) clearance?
ELVI 444 BILITRON received FDA 510(k) clearance on 1984-05-30, under 510(k) number K840757.
Who is the listed applicant for ELVI 444 BILITRON?
The FDA 510(k) record lists Logos Scientific, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ELVI 444 BILITRON?
The FDA product code for ELVI 444 BILITRON is CIG.
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 Logos Scientific, Inc. 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: CIG)
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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