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FDA 510(k)

TRANSYSTEM LIQUID STUART MEDIUM

K-Number: K924331 · 1992-12-24

ApplicantPro-Lab Diagnostics
Decision Date1992-12-24
Product CodeLIO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

TRANSYSTEM LIQUID STUART MEDIUM is the device name listed in this FDA 510(k) record. The listed applicant is Pro-Lab Diagnostics. It received FDA 510(k) clearance on 1992-12-24 under 510(k) number K924331. The device is classified under product code LIO. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRANSYSTEM LIQUID STUART MEDIUM?

TRANSYSTEM LIQUID STUART MEDIUM is a medical device that received FDA 510(k) clearance on 1992-12-24. The listed applicant is Pro-Lab Diagnostics. The 510(k) number is K924331.

When did TRANSYSTEM LIQUID STUART MEDIUM receive FDA 510(k) clearance?

TRANSYSTEM LIQUID STUART MEDIUM received FDA 510(k) clearance on 1992-12-24, under 510(k) number K924331.

Who is the listed applicant for TRANSYSTEM LIQUID STUART MEDIUM?

The FDA 510(k) record lists Pro-Lab Diagnostics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TRANSYSTEM LIQUID STUART MEDIUM?

The FDA product code for TRANSYSTEM LIQUID STUART MEDIUM is LIO.

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 Pro-Lab Diagnostics 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.

K944421E.COLI 0157 LATEX TESTK924328TRANSYSTEM LIQUID AMIES MEDIUMK924330TRANSYSTEM AMIES WITH CHARCOALK924329TRANSYSTEM AMIES W/O CHARCOAL

Related Devices (Code: LIO)

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.

K222613ARX Liquid Amies Collection & Transport SystemArx Sciences, Inc.K131630PURITAN AMIES MEDIUM COLLECTION AND TRANSPORT SYSTEMPuritan Medical Products, LLCK120846TRANSPORT CULTURE MEDIUM DEVICEPuritan Medical Products, LLCK103805MEDICAL WIRE & EQUIPMENT S-TRANSWAB (OR SIGMA-TRANSWAB) LIQUID AMIES COLLECTION AND TRANSPORT DEVICEMedical Wire & Equipment Company (Bath), Ltd.K082472VIROCULT, MODEL MW950Medical Wire & Equipment Company (Bath), Ltd.K070062COPROSET SALMONELLA AND SHIGELLA, URISET PRESERVATIVE TUBES AND SWAB SET GENERAL USEDiesse Diagnostica Senese S.P.A.

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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