OHMEDA MODEL 5330 ANESTHETIC MONITOR— 510(k) K931439

Name: FDA 510(k) clearance K931439
Creator: U.S. Food and Drug Administration
Published: 1993-10-19

Substantially Equivalent

Ohmeda Medical

FDA 510(k) clearance K931439 for OHMEDA MODEL 5330 ANESTHETIC MONITOR, Substantially Equivalent on 1993-10-19. Applicant: Ohmeda Medical. Device class: 2.

Clearance details

Applicant: Ohmeda Medical
Product code: Code CBQ
Device class: Class 2
Regulation: 21 CFR 868.1500
Advisory panel: Anesthesiology
Date received: 1993-03-22
Decision date: 1993-10-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Louisville, CO, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.