HEWLETT PACKARD M2475B CODEMASTER 100 DEFIBRILLATOR/MONITOR— 510(k) K950483

Name: FDA 510(k) clearance K950483
Creator: U.S. Food and Drug Administration
Published: 1995-05-22

Substantially Equivalent

Hewlett-Packard Co.

FDA 510(k) clearance K950483 for HEWLETT PACKARD M2475B CODEMASTER 100 DEFIBRILLATOR/MONITOR, Substantially Equivalent on 1995-05-22. Applicant: Hewlett-Packard Co.. Device class: 2.

Clearance details

Applicant: Hewlett-Packard Co.
Product code: Code DRO
Device class: Class 2
Regulation: 21 CFR 870.5550
Advisory panel: Cardiovascular
Date received: 1995-02-03
Decision date: 1995-05-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mcminnville, OR, US

Download summary PDF View on FDA.gov ↗

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