EZ-CONNECT

Set, Administration, Intravascular

VIDACARE CORPORATION

The following data is part of a premarket notification filed by Vidacare Corporation with the FDA for Ez-connect.

Pre-market Notification Details

• Device ID: K061771
• 510k Number: K061771
• Device Name: EZ-CONNECT
• Classification: Set, Administration, Intravascular
• Applicant: VIDACARE CORPORATION 3722 AVE. SAUSALITO Irvine, CA 92606
• Contact: Grace Holland
• Correspondent: Grace Holland; VIDACARE CORPORATION 3722 AVE. SAUSALITO Irvine, CA 92606
• Product Code: FPA
• CFR Regulation Number: 880.5440 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2006-06-23
• Decision Date: 2006-07-10
• Summary: summary