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FDA 510(k), K962158, PICO MODELS 30, 50, 70
FDA 510(k), K962158, PICO MODELS 30, 50, 70
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510(K) Number: K962158
Device Name: PICO MODELS 30, 50, 70
Manufacturer: RADIOMETER AMERICA, INC.
Device Classification Name: Tubes, Vials, Systems, Serum Separators, Blood Collection
Regulation Number: 862.1675
Classification Product Code: JKA
Date Received: 06/04/1996
Decision Date: 10/29/1996
Regulation Medical Specialty: Clinical Chemistry
Device Name: PICO MODELS 30, 50, 70
Manufacturer: RADIOMETER AMERICA, INC.
Device Classification Name: Tubes, Vials, Systems, Serum Separators, Blood Collection
Regulation Number: 862.1675
Classification Product Code: JKA
Date Received: 06/04/1996
Decision Date: 10/29/1996
Regulation Medical Specialty: Clinical Chemistry
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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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