FDA 510(k)

EUROMEDICAL POLY TRACHEOTOMY TUBE

K-Number: K945874 · 1994-12-27

ApplicantRegulatory & Marketing Services, Inc.

Decision Date1994-12-27

Product CodeJOH

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

EUROMEDICAL POLY TRACHEOTOMY TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Regulatory & Marketing Services, Inc.. It received FDA 510(k) clearance on 1994-12-27 under 510(k) number K945874. 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 EUROMEDICAL POLY TRACHEOTOMY TUBE?

EUROMEDICAL POLY TRACHEOTOMY TUBE is a medical device that received FDA 510(k) clearance on 1994-12-27. The listed applicant is Regulatory & Marketing Services, Inc.. The 510(k) number is K945874.

When did EUROMEDICAL POLY TRACHEOTOMY TUBE receive FDA 510(k) clearance?

EUROMEDICAL POLY TRACHEOTOMY TUBE received FDA 510(k) clearance on 1994-12-27, under 510(k) number K945874.

Who is the listed applicant for EUROMEDICAL POLY TRACHEOTOMY TUBE?

The FDA 510(k) record lists Regulatory & Marketing Services, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EUROMEDICAL POLY TRACHEOTOMY TUBE?

The FDA product code for EUROMEDICAL POLY TRACHEOTOMY TUBE 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.