VENOUS RETURN CATHETER SS-1

Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass

DLP, INC.

The following data is part of a premarket notification filed by Dlp, Inc. with the FDA for Venous Return Catheter Ss-1.

Pre-market Notification Details

• Device ID: K845045
• 510k Number: K845045
• Device Name: VENOUS RETURN CATHETER SS-1
• Classification: Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
• Applicant: DLP, INC. 620 WATSON S.W., P.O. BOX 409 Grand Rapids, MI 49501
• Contact: Ronald A Williams
• Correspondent: Ronald A Williams; DLP, INC. 620 WATSON S.W., P.O. BOX 409 Grand Rapids, MI 49501
• Product Code: DWF
• CFR Regulation Number: 870.4210 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1984-12-28
• Decision Date: 1985-04-03

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
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20613994878513	K845045	000
20613994878520	K845045	000
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