The following data is part of a premarket notification filed by Gish Biomedical, Inc. with the FDA for Soft Venous Reservoir.
Device ID | K955046 |
510k Number | K955046 |
Device Name: | SOFT VENOUS RESERVOIR |
Classification | Reservoir, Blood, Cardiopulmonary Bypass |
Applicant | GISH BIOMEDICAL, INC. 2681 KELVIN AVE. Irvine, CA 92614 -5821 |
Contact | Debra J Kridner |
Correspondent | Debra J Kridner GISH BIOMEDICAL, INC. 2681 KELVIN AVE. Irvine, CA 92614 -5821 |
Product Code | DTN |
CFR Regulation Number | 870.4400 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-11-03 |
Decision Date | 1996-01-11 |