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FDA 510(k)

LEVINE EOSIN METHYLENE BLUE AGAR

K-Number: K841142 · 1984-04-05

Decision Date1984-04-05
Product CodeJSI
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

LEVINE EOSIN METHYLENE BLUE AGAR is the device name listed in this FDA 510(k) record. The listed applicant is Anaerobe Systems. It received FDA 510(k) clearance on 1984-04-05 under 510(k) number K841142. The device is classified under product code JSI. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LEVINE EOSIN METHYLENE BLUE AGAR?

LEVINE EOSIN METHYLENE BLUE AGAR is a medical device that received FDA 510(k) clearance on 1984-04-05. The listed applicant is Anaerobe Systems. The 510(k) number is K841142.

When did LEVINE EOSIN METHYLENE BLUE AGAR receive FDA 510(k) clearance?

LEVINE EOSIN METHYLENE BLUE AGAR received FDA 510(k) clearance on 1984-04-05, under 510(k) number K841142.

Who is the listed applicant for LEVINE EOSIN METHYLENE BLUE AGAR?

The FDA 510(k) record lists Anaerobe Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LEVINE EOSIN METHYLENE BLUE AGAR?

The FDA product code for LEVINE EOSIN METHYLENE BLUE AGAR is JSI.

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 Anaerobe Systems 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.

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Related Devices (Code: JSI)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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