FDA 510(k)

REUSABLE CANNULA TRACHEOSTOMY TUBES, MODIFIED HEADS

K-Number: K936224 · 1994-08-30

Decision Date1994-08-30

Product CodeJOH

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

REUSABLE CANNULA TRACHEOSTOMY TUBES, MODIFIED HEADS is the device name listed in this FDA 510(k) record. The listed applicant is Mallinckrodt Medical Tpi, Inc.. It received FDA 510(k) clearance on 1994-08-30 under 510(k) number K936224. The device is classified under product code JOH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REUSABLE CANNULA TRACHEOSTOMY TUBES, MODIFIED HEADS?

REUSABLE CANNULA TRACHEOSTOMY TUBES, MODIFIED HEADS is a medical device that received FDA 510(k) clearance on 1994-08-30. The listed applicant is Mallinckrodt Medical Tpi, Inc.. The 510(k) number is K936224.

When did REUSABLE CANNULA TRACHEOSTOMY TUBES, MODIFIED HEADS receive FDA 510(k) clearance?

REUSABLE CANNULA TRACHEOSTOMY TUBES, MODIFIED HEADS received FDA 510(k) clearance on 1994-08-30, under 510(k) number K936224.

Who is the listed applicant for REUSABLE CANNULA TRACHEOSTOMY TUBES, MODIFIED HEADS?

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

What is the FDA product code for REUSABLE CANNULA TRACHEOSTOMY TUBES, MODIFIED HEADS?

The FDA product code for REUSABLE CANNULA TRACHEOSTOMY TUBES, MODIFIED HEADS is JOH.

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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.