SHERIDAN/ESOPHAGEAL STETHOSCOPE— 510(k) K830218

Name: FDA 510(k) clearance K830218
Creator: U.S. Food and Drug Administration
Published: 1983-03-09

Substantially Equivalent

Sheridan Catheter Corp.

FDA 510(k) clearance K830218 for SHERIDAN/ESOPHAGEAL STETHOSCOPE, Substantially Equivalent on 1983-03-09. Applicant: Sheridan Catheter Corp.. Device class: 1.

Clearance details

Applicant: Sheridan Catheter Corp.
Product code: Code BZW
Device class: Class 1
Regulation: 21 CFR 868.1910
Advisory panel: Anesthesiology
Date received: 1983-01-24
Decision date: 1983-03-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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K843070 — ESOPHAGEAL STETHOSCOPES1984-08-24
K841574 — QUAZAR ESOPHAGEAL STETHOSCOPE1984-08-15

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