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FDA 510(k), K950305, QTMICRO(TM) SYSTEM
FDA 510(k), K950305, QTMICRO(TM) SYSTEM
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510(K) Number: K950305
Device Name: QTMICRO(TM) SYSTEM
Manufacturer: Q.I. MEDICAL, INC.
Device Classification Name: set, i.v. fluid transfer
Regulation Number: 880.5440
Classification Product Code: LHI
Date Received: 01/25/1995
Decision Date: 10/13/1995
Regulation Medical Specialty: General Hospital
Device Name: QTMICRO(TM) SYSTEM
Manufacturer: Q.I. MEDICAL, INC.
Device Classification Name: set, i.v. fluid transfer
Regulation Number: 880.5440
Classification Product Code: LHI
Date Received: 01/25/1995
Decision Date: 10/13/1995
Regulation Medical Specialty: General Hospital
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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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