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FDA 510(k)

MULTIPURPOSE CULTURE MEDIUM

K-Number: K841835 · 1984-05-14

Decision Date1984-05-14
Product CodeJSG
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MULTIPURPOSE CULTURE MEDIUM is the device name listed in this FDA 510(k) record. The listed applicant is Microline Scientific. It received FDA 510(k) clearance on 1984-05-14 under 510(k) number K841835. The device is classified under product code JSG. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTIPURPOSE CULTURE MEDIUM?

MULTIPURPOSE CULTURE MEDIUM is a medical device that received FDA 510(k) clearance on 1984-05-14. The listed applicant is Microline Scientific. The 510(k) number is K841835.

When did MULTIPURPOSE CULTURE MEDIUM receive FDA 510(k) clearance?

MULTIPURPOSE CULTURE MEDIUM received FDA 510(k) clearance on 1984-05-14, under 510(k) number K841835.

Who is the listed applicant for MULTIPURPOSE CULTURE MEDIUM?

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 MULTIPURPOSE CULTURE MEDIUM?

The FDA product code for MULTIPURPOSE CULTURE MEDIUM is JSG.

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: JSG)

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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