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FDA 510(k)

FLUORTRAN - C(TM)

K-Number: K872751 · 1987-07-23

ApplicantPara Scientific Co.
Decision Date1987-07-23
Product CodeLIO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

FLUORTRAN - C(TM) is the device name listed in this FDA 510(k) record. The listed applicant is Para Scientific Co.. It received FDA 510(k) clearance on 1987-07-23 under 510(k) number K872751. 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 FLUORTRAN - C(TM)?

FLUORTRAN - C(TM) is a medical device that received FDA 510(k) clearance on 1987-07-23. The listed applicant is Para Scientific Co.. The 510(k) number is K872751.

When did FLUORTRAN - C(TM) receive FDA 510(k) clearance?

FLUORTRAN - C(TM) received FDA 510(k) clearance on 1987-07-23, under 510(k) number K872751.

Who is the listed applicant for FLUORTRAN - C(TM)?

The FDA 510(k) record lists Para Scientific Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FLUORTRAN - C(TM)?

The FDA product code for FLUORTRAN - C(TM) 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 Para Scientific Co. 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.

K021420PARACON II/FECAL CONCENTRATOR IIK964144PARACON PLUS FORMALIN - PCP-F, PARACON PLUS SAF - PCP-SAF AND PARACON PLUS MF - PCP-MFK881649MODIFIED PARACON(TM) CONCENTRATION KITK853715PARA CON TM

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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