DISSCAP HOLLOW FIBER DIALYZER

Dialyzer, Capillary, Hollow Fiber

HOSPAL MEDICAL CORP.

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

Pre-market Notification Details

Device IDK802466
510k NumberK802466
Device Name:DISSCAP HOLLOW FIBER DIALYZER
ClassificationDialyzer, Capillary, Hollow Fiber
Applicant HOSPAL MEDICAL CORP. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeFJI  
CFR Regulation Number876.5820 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1980-10-08
Decision Date1980-11-12

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