LYFO-DISK MICROORGANISMS
K-Number: K842129 · 1984-07-03
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Device Summary
Frequently Asked Questions
What is the LYFO-DISK MICROORGANISMS?
LYFO-DISK MICROORGANISMS is a medical device that received FDA 510(k) clearance on 1984-07-03. The listed applicant is Micro-Bio-Logics. The 510(k) number is K842129.
When did LYFO-DISK MICROORGANISMS receive FDA 510(k) clearance?
LYFO-DISK MICROORGANISMS received FDA 510(k) clearance on 1984-07-03, under 510(k) number K842129.
Who is the listed applicant for LYFO-DISK MICROORGANISMS?
The FDA 510(k) record lists Micro-Bio-Logics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LYFO-DISK MICROORGANISMS?
The FDA product code for LYFO-DISK MICROORGANISMS is JTR.
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 Micro-Bio-Logics 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: JTR)
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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