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FDA 510(k)

PROTECTIV 2000 I.V. CATHETER SAFETY SYSTEM

K-Number: K962226 · 1996-12-23

ApplicantJohnson & Johnson Medical, Inc.
Decision Date1996-12-23
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PROTECTIV 2000 I.V. CATHETER SAFETY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Medical, Inc.. It received FDA 510(k) clearance on 1996-12-23 under 510(k) number K962226. 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 PROTECTIV 2000 I.V. CATHETER SAFETY SYSTEM?

PROTECTIV 2000 I.V. CATHETER SAFETY SYSTEM is a medical device that received FDA 510(k) clearance on 1996-12-23. The listed applicant is Johnson & Johnson Medical, Inc.. The 510(k) number is K962226.

When did PROTECTIV 2000 I.V. CATHETER SAFETY SYSTEM receive FDA 510(k) clearance?

PROTECTIV 2000 I.V. CATHETER SAFETY SYSTEM received FDA 510(k) clearance on 1996-12-23, under 510(k) number K962226.

Who is the listed applicant for PROTECTIV 2000 I.V. CATHETER SAFETY SYSTEM?

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

What is the FDA product code for PROTECTIV 2000 I.V. CATHETER SAFETY SYSTEM?

The FDA product code for PROTECTIV 2000 I.V. CATHETER SAFETY SYSTEM 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 Johnson & Johnson Medical, 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.

K001690PROTECTIV SAFETY BLOOD COLLECTION NEEDLEK982641ADVANCED NIBP MODULEK983362NU-GEL * WOUND DRESSINGK982597FIBRCOL PLUS COLLAGEN WOUND DRESSING WITH ALGINATEK974080CRITIKON SOFT BLOOD PRESSURE CUFFK980493I.V. CATHETER SYSTEM

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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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