RODEL ELECTRODERM PADS— 510(k) K802658

Substantially Equivalent

Rodel Products Corp.

FDA 510(k) clearance K802658 for RODEL ELECTRODERM PADS, Substantially Equivalent on 1980-12-30. Applicant: Rodel Products Corp.. Device class: 2.

Clearance details

Applicant: Rodel Products Corp.
Product code: Code GYB
Device class: Class 2
Regulation: 21 CFR 882.1275
Advisory panel: Neurology
Date received: 1980-10-24
Decision date: 1980-12-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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