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FDA 510(k)

MED-WEST DUAL LUMEN INTERNAL JUGULAR CATHETER

K-Number: K905080 · 1991-01-31

ApplicantKendall Healthcare Products Co. Div.Of Tyco Health
Decision Date1991-01-31
Product CodeLFJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MED-WEST DUAL LUMEN INTERNAL JUGULAR CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Kendall Healthcare Products Co. Div.Of Tyco Health. It received FDA 510(k) clearance on 1991-01-31 under 510(k) number K905080. 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 MED-WEST DUAL LUMEN INTERNAL JUGULAR CATHETER?

MED-WEST DUAL LUMEN INTERNAL JUGULAR CATHETER is a medical device that received FDA 510(k) clearance on 1991-01-31. The listed applicant is Kendall Healthcare Products Co. Div.Of Tyco Health. The 510(k) number is K905080.

When did MED-WEST DUAL LUMEN INTERNAL JUGULAR CATHETER receive FDA 510(k) clearance?

MED-WEST DUAL LUMEN INTERNAL JUGULAR CATHETER received FDA 510(k) clearance on 1991-01-31, under 510(k) number K905080.

Who is the listed applicant for MED-WEST DUAL LUMEN INTERNAL JUGULAR CATHETER?

The FDA 510(k) record lists Kendall Healthcare Products Co. Div.Of Tyco Health as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MED-WEST DUAL LUMEN INTERNAL JUGULAR CATHETER?

The FDA product code for MED-WEST DUAL LUMEN INTERNAL JUGULAR CATHETER is LFJ.

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Other records listing Kendall Healthcare Products Co. Div.Of Tyco Health as applicant

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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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