KONTRON VITALMON 5010 PATIENT MONITOR— 510(k) K852249

Name: FDA 510(k) clearance K852249
Creator: U.S. Food and Drug Administration
Published: 1986-10-16

Substantially Equivalent

Kontron Instruments, Inc.

FDA 510(k) clearance K852249 for KONTRON VITALMON 5010 PATIENT MONITOR, Substantially Equivalent on 1986-10-16. Applicant: Kontron Instruments, Inc.. Device class: 2.

Clearance details

Applicant: Kontron Instruments, Inc.
Product code: Code BZQ
Device class: Class 2
Regulation: 21 CFR 868.2375
Advisory panel: Anesthesiology
Date received: 1985-05-23
Decision date: 1986-10-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Everett, MA, US

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