Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MULTIPURPOSE CULTURE MEDIUM

K-Number: K850733 · 1985-03-20

ApplicantRoseville Medical Laboratoriesu
Decision Date1985-03-20
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 Roseville Medical Laboratoriesu. It received FDA 510(k) clearance on 1985-03-20 under 510(k) number K850733. 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 1985-03-20. The listed applicant is Roseville Medical Laboratoriesu. The 510(k) number is K850733.

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

MULTIPURPOSE CULTURE MEDIUM received FDA 510(k) clearance on 1985-03-20, under 510(k) number K850733.

Who is the listed applicant for MULTIPURPOSE 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 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.

K850736SELECTIVE CULTURE MEDIUMK850734DIFFERENTIAL CULTURE MEDIUMK850737TRANSPORT CULTURE MEDIUMK850738SUPPLEMENT FOR CULTURE MEDIUMK850732CULTURE MEDIUM FOR PATHOGENIC NEISSERIA SSP.MIK850731CULTURE MEDIUM FOR ANTIMICROBIAL SUSCEP. TESTING

View all 8 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.

K882495THIOGLYCOLLATE BROTH W/VITA. K & HEMIN - #T3007Lakewood Biochemical Co., Inc.K881558TRYPTOSE AGARAcumedia Manufacturers, Inc.K881550OF BASAL MEDIUMAcumedia Manufacturers, Inc.K881557TRYPTONEAcumedia Manufacturers, Inc.K881564TRYPTOSE BLOOD AGAR BASE W/YEAST EXTRACTAcumedia Manufacturers, Inc.K881533BLOOD AGAR BASE NO. 2Acumedia Manufacturers, 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.

↑