STERILUCENT PROCESS CHALLENGE DEVICE— 510(k) K141312

Substantially Equivalent

Sterilucent, Inc.

FDA 510(k) clearance K141312 for STERILUCENT PROCESS CHALLENGE DEVICE, Substantially Equivalent on 2014-10-31. Applicant: Sterilucent, Inc..

Clearance details

Applicant: Sterilucent, Inc.
Product code: Code FRC
Advisory panel: General Hospital
Date received: 2014-05-20
Decision date: 2014-10-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Minneapolis, MN, US

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