MODIFIED TRACHEAL TUBE WITH SALTZMAN E.A.R.(TM)— 510(k) K870255

Name: FDA 510(k) clearance K870255
Creator: U.S. Food and Drug Administration
Published: 1987-03-26

Substantially Equivalent

Transcor, Inc.

FDA 510(k) clearance K870255 for MODIFIED TRACHEAL TUBE WITH SALTZMAN E.A.R.(TM), Substantially Equivalent on 1987-03-26. Applicant: Transcor, Inc.. Device class: 2.

Clearance details

Applicant: Transcor, Inc.
Product code: Code BZT
Device class: Class 2
Regulation: 21 CFR 868.1920
Advisory panel: Anesthesiology
Date received: 1987-01-22
Decision date: 1987-03-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: West Hartford, CT, US

Download summary PDF View on FDA.gov ↗

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