BCR-30-min BI™ and RBIP-ST30™ Readout Accessory

FDA 510(k) K151482 · Bcr Diagnostics, Inc.

Substantially Equivalent

510(k) numberK151482

Submission

Device name
BCR-30-min BI™ and RBIP-ST30™ Readout Accessory
Applicant
Bcr Diagnostics, Inc.
Phoenix, AZ, US
Received
June 2, 2015
Decision date
February 26, 2016
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FRC – Indicator, Biological Sterilization Process
Device class
Class II (moderate risk)
Regulation
21 CFR 880.2800
Specialty
General Hospital

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Questions and answers

When was BCR-30-min BI™ and RBIP-ST30™ Readout Accessory cleared by the FDA?

BCR-30-min BI™ and RBIP-ST30™ Readout Accessory (K151482) received a 510(k) decision of Substantially Equivalent on February 26, 2016, 269 days after the submission was received.

What is the product code of K151482?

The FDA product code is FRC – Indicator, Biological Sterilization Process, a Class II (moderate risk) device regulated under 21 CFR 880.2800.