EHL PULSE GENERATOR— 510(k) K931779

Substantially Equivalent

Psi Medical Products, Inc.

FDA 510(k) clearance K931779 for EHL PULSE GENERATOR, Substantially Equivalent on 1994-02-15. Applicant: Psi Medical Products, Inc..

Clearance details

Applicant: Psi Medical Products, Inc.
Product code: Code FFK
Advisory panel: Gastroenterology, Urology
Date received: 1993-04-09
Decision date: 1994-02-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shelton, CT, US

Download summary PDF View on FDA.gov ↗

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