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

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..

Clearance details

Applicant
Marketing Development Intl.
Product code
Code JOM
Advisory panel
Cardiovascular
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Mchenry, IL, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.