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FDA 510(k), K012868, MICROMEDICS FIBRIJET AEROSOL APPLICATOR
FDA 510(k), K012868, MICROMEDICS FIBRIJET AEROSOL APPLICATOR
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510(K) Number: K012868
Device Name: MICROMEDICS FIBRIJET AEROSOL APPLICATOR
Manufacturer: MICROMEDICS, INC.
Device Classification Name: syringe, piston
Regulation Number: 880.5860
Classification Product Code: FMF
Date Received: 08/27/2001
Decision Date: 10/29/2001
Regulation Medical Specialty: General Hospital
Device Name: MICROMEDICS FIBRIJET AEROSOL APPLICATOR
Manufacturer: MICROMEDICS, INC.
Device Classification Name: syringe, piston
Regulation Number: 880.5860
Classification Product Code: FMF
Date Received: 08/27/2001
Decision Date: 10/29/2001
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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