The following data is part of a premarket notification filed by Gish Biomedical, Inc. with the FDA for J-cath, Gish Model No. Jvac-xxxx.
Device ID | K863790 |
510k Number | K863790 |
Device Name: | J-CATH, GISH MODEL NO. JVAC-XXXX |
Classification | Catheter, Percutaneous |
Applicant | GISH BIOMEDICAL, INC. 2350 S. PULLMAN AVE. Santa Ana, CA 92705 |
Contact | Jeanne Pierson |
Correspondent | Jeanne Pierson GISH BIOMEDICAL, INC. 2350 S. PULLMAN AVE. Santa Ana, CA 92705 |
Product Code | DQY |
CFR Regulation Number | 870.1250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-09-26 |
Decision Date | 1987-06-24 |