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FDA 510(k)

LYFO-DISK MICROORGANISMS

K-Number: K842129 · 1984-07-03

Decision Date1984-07-03
Product CodeJTR
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

LYFO-DISK MICROORGANISMS is the device name listed in this FDA 510(k) record. The listed applicant is Micro-Bio-Logics. It received FDA 510(k) clearance on 1984-07-03 under 510(k) number K842129. The device is classified under product code JTR. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 9 devices →

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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