SOLITENS MODIFIED— 510(k) K913522

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..

Clearance details

Applicant: Innovative Designer Products, Inc.
Product code: Code GZJ
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 ↗

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