FDA 510(k), K121593, 3M ATTEST (TM) SUPER RADID READOUT STEAM CHALLENGE PACK 3M ATTEST(TM) SUPER RAPID 5 STEAM-PLUS CHALLENGE PACK

FDA 510(k), K121593, 3M ATTEST (TM) SUPER RADID READOUT STEAM CHALLENGE PACK 3M ATTEST(TM) SUPER RAPID 5 STEAM-PLUS CHALLENGE PACK

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510(K) Number: K121593
Device Name: 3M ATTEST (TM) SUPER RADID READOUT STEAM CHALLENGE PACK 3M ATTEST(TM) SUPER RAPID 5 STEAM-PLUS CHALLENGE PACK
Manufacturer:
Device Classification Name: Indicator, Biological Sterilization Process
Regulation Number: 880.2800
Classification Product Code: FRC
Date Received: 05/31/2012
Decision Date: 03/15/2013
Regulation Medical Specialty: General Hospital
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