UROMAT 2000— 510(k) K903395

Substantially Equivalent

Pausch Corp.

FDA 510(k) clearance K903395 for UROMAT 2000, Substantially Equivalent on 1990-08-30. Applicant: Pausch Corp..

Clearance details

Applicant: Pausch Corp.
Product code: Code IXR
Advisory panel: Radiology
Date received: 1990-07-27
Decision date: 1990-08-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Little Silver, NJ, US

Download summary PDF View on FDA.gov ↗

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