PLETHYSMOGRAPH (MDI SYSTEM II)— 510(k) K760504

Name: FDA 510(k) clearance K760504
Creator: U.S. Food and Drug Administration
Published: 1976-08-26

Substantially Equivalent

Marketing Development Intl.

FDA 510(k) clearance K760504 for PLETHYSMOGRAPH (MDI SYSTEM II), Substantially Equivalent on 1976-08-26. Applicant: Marketing Development Intl.. Device class: 2.

Clearance details

Applicant: Marketing Development Intl.
Product code: Code JOM
Device class: Class 2
Regulation: 21 CFR 870.2780
Advisory panel: Cardiovascular
Date received: 1976-08-23
Decision date: 1976-08-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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