SOLITENS MODIFIED— 510(k) K913522

Name: FDA 510(k) clearance K913522
Creator: U.S. Food and Drug Administration
Published: 1991-08-28

Substantially Equivalent

Innovative Designer Products, Inc.

FDA 510(k) clearance K913522 for SOLITENS MODIFIED, Substantially Equivalent on 1991-08-28. Applicant: Innovative Designer Products, Inc.. Device class: 2.

Clearance details

Applicant: Innovative Designer Products, Inc.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1991-07-26
Decision date: 1991-08-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Glen Rock, NJ, 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.