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FDA 510(k)

DESERET SUBCLAVIAN HEMODIALYSIS CATHETER

K-Number: K881695 · 1988-06-23

ApplicantDeseret Medical, Inc.
Decision Date1988-06-23
Product CodeLFJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DESERET SUBCLAVIAN HEMODIALYSIS 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 1988-06-23 under 510(k) number K881695. The device is classified under product code LFJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DESERET SUBCLAVIAN HEMODIALYSIS CATHETER?

DESERET SUBCLAVIAN HEMODIALYSIS CATHETER is a medical device that received FDA 510(k) clearance on 1988-06-23. The listed applicant is Deseret Medical, Inc.. The 510(k) number is K881695.

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

DESERET SUBCLAVIAN HEMODIALYSIS CATHETER received FDA 510(k) clearance on 1988-06-23, under 510(k) number K881695.

Who is the listed applicant for DESERET SUBCLAVIAN HEMODIALYSIS 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 SUBCLAVIAN HEMODIALYSIS CATHETER?

The FDA product code for DESERET SUBCLAVIAN HEMODIALYSIS CATHETER is LFJ.

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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: LFJ)

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.

K920780MEDSURG INSERTION TRAYMedsurg Industries, Inc.K925819AKCESS0CATH KITAkcess Medical Products, Inc.K925818AKCESS-CATHAkcess Medical Products, Inc.K913468ULDALL DOUBLE LUMEN HEMODIALYSIS CATHETER SET/TRAYCook, Inc.K931120COAXIAL ACUTE CATHETERAkcess Medical Products, Inc.K920634SPLITTABLE SHEATH INTRODUCER SETAkcess Medical Products, 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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