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FDA 510(k)

DIFFERENTIAL CULTURE MEDIUM

K-Number: K850734 · 1985-03-20

ApplicantRoseville Medical Laboratoriesu
Decision Date1985-03-20
Product CodeJSE
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

DIFFERENTIAL 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 K850734. The device is classified under product code JSE. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIFFERENTIAL CULTURE MEDIUM?

DIFFERENTIAL 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 K850734.

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

DIFFERENTIAL CULTURE MEDIUM received FDA 510(k) clearance on 1985-03-20, under 510(k) number K850734.

Who is the listed applicant for DIFFERENTIAL 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 DIFFERENTIAL CULTURE MEDIUM?

The FDA product code for DIFFERENTIAL CULTURE MEDIUM is JSE.

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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.

K850733MULTIPURPOSE CULTURE MEDIUMK850736SELECTIVE CULTURE MEDIUMK850737TRANSPORT CULTURE MEDIUMK850738SUPPLEMENT FOR CULTURE MEDIUMK850732CULTURE MEDIUM FOR PATHOGENIC NEISSERIA SSP.MIK850731CULTURE MEDIUM FOR ANTIMICROBIAL SUSCEP. TESTING

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Related Devices (Code: JSE)

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.

K962265MLX MICROTITER PLATE LUMINOMETERDynatech Laboratories, Inc.K883995X-ACT UREA/TDAPro-Lab, Inc.K883996X-ACT LDC/INDPro-Lab, Inc.K880133MIL MEDIUMHardy MediaK880116MRVP BROTHHardy MediaK874537KLIGLER IRON AGAR AND TRIPLE SUGAR IRON AGARLakewood Biochemical Co., Inc.

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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