SALTZMAN EAR(TM) ENDOTRACHEAL ASCULTATION RECEPTOR— 510(k) K862131

Name: FDA 510(k) clearance K862131
Creator: U.S. Food and Drug Administration
Published: 1986-07-14

Substantially Equivalent

K & S Medicorp

FDA 510(k) clearance K862131 for SALTZMAN EAR(TM) ENDOTRACHEAL ASCULTATION RECEPTOR, Substantially Equivalent on 1986-07-14. Applicant: K & S Medicorp. Device class: 2.

Clearance details

Applicant: K & S Medicorp
Product code: Code BZT
Device class: Class 2
Regulation: 21 CFR 868.1920
Advisory panel: Anesthesiology
Date received: 1986-06-04
Decision date: 1986-07-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Miami, FL, US

Download summary PDF View on FDA.gov ↗

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