VENOUS CANNULA W/BENT, TIP WIRE

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 Cannula W/bent, Tip Wire.

Pre-market Notification Details

• Device ID: K842375
• 510k Number: K842375
• Device Name: VENOUS CANNULA W/BENT, TIP WIRE
• Classification: Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
• Applicant: DLP, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050
• Product Code: DWF
• CFR Regulation Number: 870.4210 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1984-06-18
• Decision Date: 1984-08-10

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
20613994878315	K842375	000
20613994878445	K842375	000
20613994878452	K842375	000
20613994878469	K842375	000
20613994878476	K842375	000
20613994879121	K842375	000
20613994879138	K842375	000
20613994879152	K842375	000
20613994879169	K842375	000
20613994878421	K842375	000
20613994878414	K842375	000
20613994878407	K842375	000
20613994878322	K842375	000
20613994878339	K842375	000
20613994878346	K842375	000
20613994878353	K842375	000
20613994878360	K842375	000
20613994878377	K842375	000
20613994878384	K842375	000
20613994878391	K842375	000
20613994879176	K842375	000
20613994879183	K842375	000
20613994879206	K842375	000
20613994879329	K842375	000
20643169083763	K842375	000
20643169086634	K842375	000
20643169086641	K842375	000
00673978861869	K842375	000
00643169160118	K842375	000
00643169160125	K842375	000
00643169160132	K842375	000
20613994879312	K842375	000
20613994879305	K842375	000
20613994879299	K842375	000
20613994879213	K842375	000
20613994879220	K842375	000
20613994879237	K842375	000
20613994879244	K842375	000
20613994879251	K842375	000
20613994879268	K842375	000
20613994879275	K842375	000
20613994879282	K842375	000
20613994878438	K842375	000