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FDA 510(k)

CAREKITS(TM), IV/CATH/CENT LINE DRESS/TPN/CVP KITS

K-Number: K903545 · 1990-11-13

ApplicantJ.J. Skinner, Inc.
Decision Date1990-11-13
Product CodeFOZ
Advisory CommitteeHO
DecisionUnknown

Device Summary

CAREKITS(TM), IV/CATH/CENT LINE DRESS/TPN/CVP KITS is the device name listed in this FDA 510(k) record. The listed applicant is J.J. Skinner, Inc.. It received FDA 510(k) clearance on 1990-11-13 under 510(k) number K903545. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the CAREKITS(TM), IV/CATH/CENT LINE DRESS/TPN/CVP KITS?

CAREKITS(TM), IV/CATH/CENT LINE DRESS/TPN/CVP KITS is a medical device that received FDA 510(k) clearance on 1990-11-13. The listed applicant is J.J. Skinner, Inc.. The 510(k) number is K903545.

When did CAREKITS(TM), IV/CATH/CENT LINE DRESS/TPN/CVP KITS receive FDA 510(k) clearance?

CAREKITS(TM), IV/CATH/CENT LINE DRESS/TPN/CVP KITS received FDA 510(k) clearance on 1990-11-13, under 510(k) number K903545.

Who is the listed applicant for CAREKITS(TM), IV/CATH/CENT LINE DRESS/TPN/CVP KITS?

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

What is the FDA product code for CAREKITS(TM), IV/CATH/CENT LINE DRESS/TPN/CVP KITS?

The FDA product code for CAREKITS(TM), IV/CATH/CENT LINE DRESS/TPN/CVP KITS is FOZ.

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Other records listing J.J. Skinner, 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.

K961227JJ SKINNER CAREKITS WOUND CARE MANAGEMENT/DRESSING CHANGE TRAYK961683JJ SKINNER CAREKITS MINOR SURGICAL PROCEDURE TRAYK925469JJ SKINNER CAREKITS(TM) DIALYSIS ON/OFF KITK925467JJ SKINNER CAREKITS(TM) DRY/WET/GEL SKIN SCRUB KITK925468JJ SKINNER CAREKITS(TM) BLOOD COLLECTION KITK903544CAREKITS(TM) INCISION/DRAINAGE/SUTURE REMOVAL KITS

View all 7 devices →

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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