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FDA 510(k)

SELECTIVE CULTURE MEDIUM

K-Number: K850736 · 1985-03-20

Decision Date1985-03-20
Product CodeJSI
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

SELECTIVE CULTURE MEDIUM is the device name listed in this FDA 510(k) record. The listed applicant is Roseville Medical Laboratoriesu. It received FDA 510(k) clearance on 1985-03-20 under 510(k) number K850736. 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 SELECTIVE CULTURE MEDIUM?

SELECTIVE CULTURE MEDIUM is a medical device that received FDA 510(k) clearance on 1985-03-20. The listed applicant is Roseville Medical Laboratoriesu. The 510(k) number is K850736.

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

SELECTIVE CULTURE MEDIUM received FDA 510(k) clearance on 1985-03-20, under 510(k) number K850736.

Who is the listed applicant for SELECTIVE CULTURE MEDIUM?

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

What is the FDA product code for SELECTIVE CULTURE MEDIUM?

The FDA product code for SELECTIVE CULTURE MEDIUM 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 Roseville Medical Laboratoriesu 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 8 devices →

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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