MODIFIED RUBAGEN— 510(k) K896433

Substantially Equivalent

Biokit USA, Inc.

FDA 510(k) clearance K896433 for MODIFIED RUBAGEN, Substantially Equivalent on 1989-11-29. Applicant: Biokit USA, Inc..

Clearance details

Applicant: Biokit USA, Inc.
Product code: Code LQN
Advisory panel: Microbiology
Date received: 1989-11-09
Decision date: 1989-11-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Barcelona, ES

Download summary PDF View on FDA.gov ↗

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