TENZCARE DUAL-CHANNEL STIMULATOR— 510(k) K800758

Substantially Equivalent

3M Company

FDA 510(k) clearance K800758 for TENZCARE DUAL-CHANNEL STIMULATOR, Substantially Equivalent on 1980-04-10. Applicant: 3M Company.

Clearance details

Applicant
3M Company
Product code
Code GZJ
Advisory panel
Neurology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
White City, OR, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.