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FDA 510(k)

DIFFERENTIAL CULTURE MED. LEVINE EMB

K-Number: K841843 · 1984-05-31

Decision Date1984-05-31
Product CodeJSH
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

DIFFERENTIAL CULTURE MED. LEVINE EMB is the device name listed in this FDA 510(k) record. The listed applicant is Microline Scientific. It received FDA 510(k) clearance on 1984-05-31 under 510(k) number K841843. The device is classified under product code JSH. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIFFERENTIAL CULTURE MED. LEVINE EMB?

DIFFERENTIAL CULTURE MED. LEVINE EMB is a medical device that received FDA 510(k) clearance on 1984-05-31. The listed applicant is Microline Scientific. The 510(k) number is K841843.

When did DIFFERENTIAL CULTURE MED. LEVINE EMB receive FDA 510(k) clearance?

DIFFERENTIAL CULTURE MED. LEVINE EMB received FDA 510(k) clearance on 1984-05-31, under 510(k) number K841843.

Who is the listed applicant for DIFFERENTIAL CULTURE MED. LEVINE EMB?

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

What is the FDA product code for DIFFERENTIAL CULTURE MED. LEVINE EMB?

The FDA product code for DIFFERENTIAL CULTURE MED. LEVINE EMB is JSH.

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 Microline Scientific 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 14 devices →

Related Devices (Code: JSH)

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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