SEROJET— 510(k) K003908

Substantially Equivalent

Bioject, Inc.

FDA 510(k) clearance K003908 for SEROJET, Substantially Equivalent on 2001-03-08. Applicant: Bioject, Inc..

Clearance details

Applicant: Bioject, Inc.
Product code: Code KZE
Advisory panel: General Hospital
Date received: 2000-12-19
Decision date: 2001-03-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Portland, OR, US

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