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FDA 510(k)

URINE CULTUR STABILIZATION TRANSPORT TUBE

K-Number: K920761 · 1992-06-19

ApplicantBio Medicus, Inc.
Decision Date1992-06-19
Product CodeLIO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

URINE CULTUR STABILIZATION TRANSPORT TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Bio Medicus, Inc.. It received FDA 510(k) clearance on 1992-06-19 under 510(k) number K920761. 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 URINE CULTUR STABILIZATION TRANSPORT TUBE?

URINE CULTUR STABILIZATION TRANSPORT TUBE is a medical device that received FDA 510(k) clearance on 1992-06-19. The listed applicant is Bio Medicus, Inc.. The 510(k) number is K920761.

When did URINE CULTUR STABILIZATION TRANSPORT TUBE receive FDA 510(k) clearance?

URINE CULTUR STABILIZATION TRANSPORT TUBE received FDA 510(k) clearance on 1992-06-19, under 510(k) number K920761.

Who is the listed applicant for URINE CULTUR STABILIZATION TRANSPORT TUBE?

The FDA 510(k) record lists Bio Medicus, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for URINE CULTUR STABILIZATION TRANSPORT TUBE?

The FDA product code for URINE CULTUR STABILIZATION TRANSPORT TUBE is LIO.

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Other records listing Bio Medicus, Inc. 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.

K903410BIO-MEDICUS CANNULA INTRODUCERK901253(PBS) PORTABLE BYPASS SYSTEM, MODEL 1000K901584BIO-MEDICUS BIO CONSOLE MODELS 540 A B CK894980BIO-CAL 370 HEATER/COOLERK884129BIO-MEDICUS PERCUTANEOUS CANNULA & INTRODUCER SETK883956BIO-MEDICUS TUBING CONNECTORS

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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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