DeviceClearance

PATHWAY II ELECTROMYOGRAPH— 510(k) K897132

Substantially Equivalent

The Prometheus Group

FDA 510(k) clearance K897132 for PATHWAY II ELECTROMYOGRAPH, Substantially Equivalent on 1991-04-18. Applicant: The Prometheus Group.

Clearance details

Applicant
The Prometheus Group
Product code
Code HCC
Advisory panel
Neurology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Portsmouth, NH, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.