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 ID: K823707
• 510k Number: K823707
• Device Name: HOSPAL BLOOD LINES
• Classification: Accessories, Blood Circuit, Hemodialysis
• Applicant: HOSPAL MEDICAL CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050
• Product Code: KOC
• CFR Regulation Number: 876.5820 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1982-12-09
• Decision Date: 1983-01-05

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
37332414075430	K823707	000
37332414044733	K823707	000
37332414032532	K823707	000
37332414010868	K823707	000