1-4F INFINITI ANGIOGRAPHIC CATHETER

Catheter, Intravascular, Diagnostic

CORDIS CORP.

The following data is part of a premarket notification filed by Cordis Corp. with the FDA for 1-4f Infiniti Angiographic Catheter.

Pre-market Notification Details

• Device ID: K960975
• 510k Number: K960975
• Device Name: 1-4F INFINITI ANGIOGRAPHIC CATHETER
• Classification: Catheter, Intravascular, Diagnostic
• Applicant: CORDIS CORP. 14201 N.W. 60TH AVE. Miami Lakes, FL 33014
• Contact: Jodi Lynn Frasier
• Correspondent: Jodi Lynn Frasier; CORDIS CORP. 14201 N.W. 60TH AVE. Miami Lakes, FL 33014
• Product Code: DQO
• CFR Regulation Number: 870.1200 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1996-03-11
• Decision Date: 1996-04-02
• Summary: summary

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
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