FDA 510(k)

DUAL-LUMEN LONG TERM CENTRAL VENOUS CAT

K-Number: K834383 · 1984-05-01

Decision Date1984-05-01

Product CodeLJS

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

DUAL-LUMEN LONG TERM CENTRAL VENOUS CAT is the device name listed in this FDA 510(k) record. The listed applicant is Burron Medical Products, Inc.. It received FDA 510(k) clearance on 1984-05-01 under 510(k) number K834383. The device is classified under product code LJS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUAL-LUMEN LONG TERM CENTRAL VENOUS CAT?

DUAL-LUMEN LONG TERM CENTRAL VENOUS CAT is a medical device that received FDA 510(k) clearance on 1984-05-01. The listed applicant is Burron Medical Products, Inc.. The 510(k) number is K834383.

When did DUAL-LUMEN LONG TERM CENTRAL VENOUS CAT receive FDA 510(k) clearance?

DUAL-LUMEN LONG TERM CENTRAL VENOUS CAT received FDA 510(k) clearance on 1984-05-01, under 510(k) number K834383.

Who is the listed applicant for DUAL-LUMEN LONG TERM CENTRAL VENOUS CAT?

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

What is the FDA product code for DUAL-LUMEN LONG TERM CENTRAL VENOUS CAT?

The FDA product code for DUAL-LUMEN LONG TERM CENTRAL VENOUS CAT is LJS.

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Other records listing Burron Medical Products, Inc. as applicant

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Related Devices (Code: LJS)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.