THERASTIM— 510(k) K914813

Substantially Equivalent

Precision Electronics , Ltd.

FDA 510(k) clearance K914813 for THERASTIM, Substantially Equivalent on 1991-12-31. Applicant: Precision Electronics , Ltd.. Device class: 2.

Clearance details

Applicant: Precision Electronics , Ltd.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1991-10-25
Decision date: 1991-12-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Montclair, CA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.