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FDA 510(k)

SUPPLEMENT FOR CULTURE MEDIUM

K-Number: K850738 · 1985-03-20

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

Device Summary

SUPPLEMENT FOR 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 K850738. The device is classified under product code JSK. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUPPLEMENT FOR CULTURE MEDIUM?

SUPPLEMENT FOR 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 K850738.

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

SUPPLEMENT FOR CULTURE MEDIUM received FDA 510(k) clearance on 1985-03-20, under 510(k) number K850738.

Who is the listed applicant for SUPPLEMENT FOR 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 SUPPLEMENT FOR CULTURE MEDIUM?

The FDA product code for SUPPLEMENT FOR CULTURE MEDIUM is JSK.

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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 MEDIUMK850734DIFFERENTIAL CULTURE MEDIUMK850737TRANSPORT CULTURE MEDIUMK850732CULTURE MEDIUM FOR PATHOGENIC NEISSERIA SSP.MIK850731CULTURE MEDIUM FOR ANTIMICROBIAL SUSCEP. TESTING

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Related Devices (Code: JSK)

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.

K881949ATS NAC-PAC SETAlpha-Tec Systems, Inc.K881879ATS M/15 PHOSPHATE BUFFER, PRODUCT #034-42Alpha-Tec Systems, Inc.K881566HEMOGLOBIN POWDERAcumedia Manufacturers, Inc.K861997PENICILLIN-STREPTOMYCIN-FUNGIZONE MIXTUREHazleton Research Products, Inc.K861791PENICILLIN-STREPTOMYCIN-FUNGIZONEFlow Laboratories, Inc.K861824GENTAMICIN SULFATE SOLUTION (10MG GENTAMICIN)Flow Laboratories, 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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