DURACATH— 510(k) K901133

Substantially Equivalent

Impra, Inc.

FDA 510(k) clearance K901133 for DURACATH, Substantially Equivalent on 1990-06-08. Applicant: Impra, Inc..

Clearance details

Applicant: Impra, Inc.
Product code: Code LFJ
Advisory panel: Gastroenterology, Urology
Date received: 1990-03-12
Decision date: 1990-06-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tempe, AZ, US

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