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FDA 510(k)

NU-CATH EMERGENCY KIT

K-Number: K850398 · 1985-03-27

ApplicantIntl. Medical Devices , Ltd.
Decision Date1985-03-27
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NU-CATH EMERGENCY KIT is the device name listed in this FDA 510(k) record. The listed applicant is Intl. Medical Devices , Ltd.. It received FDA 510(k) clearance on 1985-03-27 under 510(k) number K850398. 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 NU-CATH EMERGENCY KIT?

NU-CATH EMERGENCY KIT is a medical device that received FDA 510(k) clearance on 1985-03-27. The listed applicant is Intl. Medical Devices , Ltd.. The 510(k) number is K850398.

When did NU-CATH EMERGENCY KIT receive FDA 510(k) clearance?

NU-CATH EMERGENCY KIT received FDA 510(k) clearance on 1985-03-27, under 510(k) number K850398.

Who is the listed applicant for NU-CATH EMERGENCY KIT?

The FDA 510(k) record lists Intl. Medical Devices , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NU-CATH EMERGENCY KIT?

The FDA product code for NU-CATH EMERGENCY KIT is FOZ.

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Other records listing Intl. Medical Devices , Ltd. 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.

K913540PEDIA-THOR THORACOSTOMY KITK913541NEO-THOR THORACOSTOMY KITK913542THORACIC CATHETER WITH GUIDEK913539THORACIC CATHTER STYLETK913543THORACIC CATHETER STYLETK862909RE-TRAKE WEISS EMERGENCY AIRWAY & THORACIC 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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