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FDA 510(k), K800666, QUIK-TEMP
FDA 510(k), K800666, QUIK-TEMP
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$149.00 USD
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$149.00 USD
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510(K) Number: K800666
Device Name: QUIK-TEMP
Manufacturer: LIQUID CRYSTAL PRODUCTS, INC.
Device Classification Name: peritoneal dialysate filter
Regulation Number: 876.5630
Classification Product Code: KPP
Date Received: 03/26/1980
Decision Date: 05/08/1980
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: QUIK-TEMP
Manufacturer: LIQUID CRYSTAL PRODUCTS, INC.
Device Classification Name: peritoneal dialysate filter
Regulation Number: 876.5630
Classification Product Code: KPP
Date Received: 03/26/1980
Decision Date: 05/08/1980
Regulation Medical Specialty: Gastroenterology/Urology
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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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