HOSPAL BLOOD LINES

Accessories, Blood Circuit, Hemodialysis

HOSPAL MEDICAL CORP.

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

Pre-market Notification Details

Device IDK823707
510k NumberK823707
Device Name:HOSPAL BLOOD LINES
ClassificationAccessories, Blood Circuit, Hemodialysis
Applicant HOSPAL MEDICAL CORP. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeKOC  
CFR Regulation Number876.5820 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1982-12-09
Decision Date1983-01-05

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
37332414075430 K823707 000
37332414044733 K823707 000
37332414032532 K823707 000
37332414010868 K823707 000

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.