DISSCAP 110

System, Dialysate Delivery, Central Multiple Patient

HOSPAL MEDICAL CORP.

The following data is part of a premarket notification filed by Hospal Medical Corp. with the FDA for Disscap 110.

Pre-market Notification Details

Device IDK820966
510k NumberK820966
Device Name:DISSCAP 110
ClassificationSystem, Dialysate Delivery, Central Multiple Patient
Applicant HOSPAL MEDICAL CORP. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeFKQ  
CFR Regulation Number876.5820 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1982-04-06
Decision Date1982-04-16

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