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FDA 510(k)

DESERET SPLITTABLE CATHETER

K-Number: K874582 · 1987-12-29

ApplicantDeseret Medical, Inc.
Decision Date1987-12-29
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DESERET SPLITTABLE CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Deseret Medical, Inc.. It received FDA 510(k) clearance on 1987-12-29 under 510(k) number K874582. 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 DESERET SPLITTABLE CATHETER?

DESERET SPLITTABLE CATHETER is a medical device that received FDA 510(k) clearance on 1987-12-29. The listed applicant is Deseret Medical, Inc.. The 510(k) number is K874582.

When did DESERET SPLITTABLE CATHETER receive FDA 510(k) clearance?

DESERET SPLITTABLE CATHETER received FDA 510(k) clearance on 1987-12-29, under 510(k) number K874582.

Who is the listed applicant for DESERET SPLITTABLE CATHETER?

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

What is the FDA product code for DESERET SPLITTABLE CATHETER?

The FDA product code for DESERET SPLITTABLE CATHETER is FOZ.

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Other records listing Deseret 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.

K913027VESSEL DILATORK904648SAFE SYTE I.V. CATHETER PLACEMENT UNITK904121VIALON OBTURATORK904122INSYTE-A ARTERIAL CATHETERIZATION UNITK900116DESERET OPTIMA INTRAVASCULAR CATHETERK895735DESERET MULTILUMEN SUBCLAVIAN CATHETER

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Related Devices (Code: FOZ)

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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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