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FDA 510(k)

ACCI-GUARD(TM) I.V. CATHETER PLACEMENT UNIT

K-Number: K890751 · 1989-04-21

ApplicantMedical Safety Products, Inc.
Decision Date1989-04-21
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ACCI-GUARD(TM) I.V. CATHETER PLACEMENT UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Medical Safety Products, Inc.. It received FDA 510(k) clearance on 1989-04-21 under 510(k) number K890751. 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 ACCI-GUARD(TM) I.V. CATHETER PLACEMENT UNIT?

ACCI-GUARD(TM) I.V. CATHETER PLACEMENT UNIT is a medical device that received FDA 510(k) clearance on 1989-04-21. The listed applicant is Medical Safety Products, Inc.. The 510(k) number is K890751.

When did ACCI-GUARD(TM) I.V. CATHETER PLACEMENT UNIT receive FDA 510(k) clearance?

ACCI-GUARD(TM) I.V. CATHETER PLACEMENT UNIT received FDA 510(k) clearance on 1989-04-21, under 510(k) number K890751.

Who is the listed applicant for ACCI-GUARD(TM) I.V. CATHETER PLACEMENT UNIT?

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

What is the FDA product code for ACCI-GUARD(TM) I.V. CATHETER PLACEMENT UNIT?

The FDA product code for ACCI-GUARD(TM) I.V. CATHETER PLACEMENT UNIT 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 Medical Safety Products, 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.

K942624LOK-ON NEEDLE DISPOSAL CONTAINERK913329V-ACCI-GUARD(TM) REUSABLE HOLDERK895075ACCI-GUARD REUSABLE HOLDERK884139ACCI-GUARD(TM) REGULAR AND PEDIATRIC HOLDERK881654ACCI-GUARD MULTI-SAMPLE BLOOD COLLECTION NEEDLE

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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