ELECTRONIC PACEMAKER WAVEFORM ANALYZER— 510(k) K800696

Substantially Equivalent

Instromedix, Inc.

FDA 510(k) clearance K800696 for ELECTRONIC PACEMAKER WAVEFORM ANALYZER, Substantially Equivalent on 1980-08-14. Applicant: Instromedix, Inc..

Clearance details

Applicant: Instromedix, Inc.
Product code: Code KRE
Advisory panel: Cardiovascular
Date received: 1980-03-28
Decision date: 1980-08-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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