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FDA 510(k), K982151, STERITITE PROCESS INDICATOR ACCESSORIES
FDA 510(k), K982151, STERITITE PROCESS INDICATOR ACCESSORIES
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510(K) Number: K982151
Device Name: STERITITE PROCESS INDICATOR ACCESSORIES
Manufacturer: MARCIA FRIEZE
Device Classification Name: Indicator, Physical/Chemical Sterilization Process
Regulation Number: JOJ
Classification Product Code: 06/18/1998
Date Received: 02/09/1999
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
Device Name: STERITITE PROCESS INDICATOR ACCESSORIES
Manufacturer: MARCIA FRIEZE
Device Classification Name: Indicator, Physical/Chemical Sterilization Process
Regulation Number: JOJ
Classification Product Code: 06/18/1998
Date Received: 02/09/1999
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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