FDA 510(k)

L-F COILED EXTENSION TUBING

K-Number: K882329 · 1988-09-02

Decision Date1988-09-02

Product CodeDXT

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

L-F COILED EXTENSION TUBING is the device name listed in this FDA 510(k) record. The listed applicant is Mallinckrodt Group, Inc.. It received FDA 510(k) clearance on 1988-09-02 under 510(k) number K882329. The device is classified under product code DXT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the L-F COILED EXTENSION TUBING?

L-F COILED EXTENSION TUBING is a medical device that received FDA 510(k) clearance on 1988-09-02. The listed applicant is Mallinckrodt Group, Inc.. The 510(k) number is K882329.

When did L-F COILED EXTENSION TUBING receive FDA 510(k) clearance?

L-F COILED EXTENSION TUBING received FDA 510(k) clearance on 1988-09-02, under 510(k) number K882329.

Who is the listed applicant for L-F COILED EXTENSION TUBING?

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

What is the FDA product code for L-F COILED EXTENSION TUBING?

The FDA product code for L-F COILED EXTENSION TUBING is DXT.

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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.