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FDA 510(k)

BT CATH (INTRAVASCULAR CATHETER)

K-Number: K862480 · 1986-07-31

ApplicantBaron Technologies, Inc.
Decision Date1986-07-31
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BT CATH (INTRAVASCULAR CATHETER) is the device name listed in this FDA 510(k) record. The listed applicant is Baron Technologies, Inc.. It received FDA 510(k) clearance on 1986-07-31 under 510(k) number K862480. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BT CATH (INTRAVASCULAR CATHETER)?

BT CATH (INTRAVASCULAR CATHETER) is a medical device that received FDA 510(k) clearance on 1986-07-31. The listed applicant is Baron Technologies, Inc.. The 510(k) number is K862480.

When did BT CATH (INTRAVASCULAR CATHETER) receive FDA 510(k) clearance?

BT CATH (INTRAVASCULAR CATHETER) received FDA 510(k) clearance on 1986-07-31, under 510(k) number K862480.

Who is the listed applicant for BT CATH (INTRAVASCULAR CATHETER)?

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

What is the FDA product code for BT CATH (INTRAVASCULAR CATHETER)?

The FDA product code for BT CATH (INTRAVASCULAR CATHETER) is FOZ.

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 Baron Technologies, 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.

K864541BT HYPODERMIC SYRINGE

Related Devices (Code: FOZ)

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.

K260432Ruby Intravascular CatheterVenocare, Inc.K260165Unimpregnated Central Venous CatheterSpectrum VascularK261041ClearSafe Closed SystemMedSource Labs, LLCK260539MedSource QuickSafe™ Safety IV Catheter; MedSource PurSafe™ Safety IV CatheterMedSource Labs, LLCK253235Introcan Safety® Deep Access XL IV CatheterB.Braun Medical, Inc.K252137BD Insyte™ IV CatheterBecton Dickinson Infusion Therapy Systems, 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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