KONTRON CUTANEOUS PO2 MONITOR 820— 510(k) K860951

Name: FDA 510(k) clearance K860951
Creator: U.S. Food and Drug Administration
Published: 1986-04-09

Substantially Equivalent

Kontron Instruments, Inc.

FDA 510(k) clearance K860951 for KONTRON CUTANEOUS PO2 MONITOR 820, Substantially Equivalent on 1986-04-09. Applicant: Kontron Instruments, Inc.. Device class: 2.

Clearance details

Applicant: Kontron Instruments, Inc.
Product code: Code KLK
Device class: Class 2
Regulation: 21 CFR 868.2500
Advisory panel: Anesthesiology
Date received: 1986-03-12
Decision date: 1986-04-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Everett, MA, US

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