C-PORT

Port & Catheter, Implanted, Subcutaneous, Intravascular

CLINISURG VASCULAR PRODUCTS, LLC

The following data is part of a premarket notification filed by Clinisurg Vascular Products, Llc with the FDA for C-port.

Pre-market Notification Details

• Device ID: K030636
• 510k Number: K030636
• Device Name: C-PORT
• Classification: Port & Catheter, Implanted, Subcutaneous, Intravascular
• Applicant: CLINISURG VASCULAR PRODUCTS, LLC 5454 AMESBURY DR., #2107 Dallas, TX 75206
• Contact: Donald F Hults
• Correspondent: Donald F Hults; CLINISURG VASCULAR PRODUCTS, LLC 5454 AMESBURY DR., #2107 Dallas, TX 75206
• Product Code: LJT
• CFR Regulation Number: 880.5965 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2003-02-28
• Decision Date: 2003-06-05
• Summary: summary