IV HOUSE

Device, Intravascular Catheter Securement

PROGRESSIVE IV'S, INC.

The following data is part of a premarket notification filed by Progressive Iv's, Inc. with the FDA for Iv House.

Pre-market Notification Details

• Device ID: K912942
• 510k Number: K912942
• Device Name: IV HOUSE
• Classification: Device, Intravascular Catheter Securement
• Applicant: PROGRESSIVE IV'S, INC. 7400 FOXMONT DR. Hazelwood, MO 63042 -2198
• Contact: Bett M Rozier
• Correspondent: Bett M Rozier; PROGRESSIVE IV'S, INC. 7400 FOXMONT DR. Hazelwood, MO 63042 -2198
• Product Code: KMK
• CFR Regulation Number: 880.5210 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1991-07-03
• Decision Date: 1991-09-25