INTRADUCER

Catheter, Peritoneal

TAUT, INC.

The following data is part of a premarket notification filed by Taut, Inc. with the FDA for Intraducer.

Pre-market Notification Details

• Device ID: K992907
• 510k Number: K992907
• Device Name: INTRADUCER
• Classification: Catheter, Peritoneal
• Applicant: TAUT, INC. 2571 KANEVILLE COURT P.O. BOX 326 Geneva, IL 60134
• Contact: Ronald Kenseth
• Correspondent: Ronald Kenseth; TAUT, INC. 2571 KANEVILLE COURT P.O. BOX 326 Geneva, IL 60134
• Product Code: GBW
• CFR Regulation Number: 878.4200 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1999-08-30
• Decision Date: 1999-10-05