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FDA 510(k)

DIXIE USA PTL, PHARYNGEAL TRACHEAL LUMEN

K-Number: K831481 · 1983-10-04

ApplicantEugene Scarberry
Decision Date1983-10-04
Product CodeDSK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DIXIE USA PTL, PHARYNGEAL TRACHEAL LUMEN is the device name listed in this FDA 510(k) record. The listed applicant is Eugene Scarberry. It received FDA 510(k) clearance on 1983-10-04 under 510(k) number K831481. The device is classified under product code DSK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIXIE USA PTL, PHARYNGEAL TRACHEAL LUMEN?

DIXIE USA PTL, PHARYNGEAL TRACHEAL LUMEN is a medical device that received FDA 510(k) clearance on 1983-10-04. The listed applicant is Eugene Scarberry. The 510(k) number is K831481.

When did DIXIE USA PTL, PHARYNGEAL TRACHEAL LUMEN receive FDA 510(k) clearance?

DIXIE USA PTL, PHARYNGEAL TRACHEAL LUMEN received FDA 510(k) clearance on 1983-10-04, under 510(k) number K831481.

Who is the listed applicant for DIXIE USA PTL, PHARYNGEAL TRACHEAL LUMEN?

The FDA 510(k) record lists Eugene Scarberry as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIXIE USA PTL, PHARYNGEAL TRACHEAL LUMEN?

The FDA product code for DIXIE USA PTL, PHARYNGEAL TRACHEAL LUMEN is DSK.

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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.

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