PULSATOR 5000— 510(k) K930102

Substantially Equivalent

Toys House Industrial Corp.

FDA 510(k) clearance K930102 for PULSATOR 5000, Substantially Equivalent on 1994-03-23. Applicant: Toys House Industrial Corp.. Device class: 2.

Clearance details

Applicant: Toys House Industrial Corp.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1993-01-08
Decision date: 1994-03-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Great Neck, NY, 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.