The following data is part of a premarket notification filed by Go Medical Industries Pty. Ltd. with the FDA for The O'neil Sterile Field Urinary Catheter Kit.
Device ID | K002803 |
510k Number | K002803 |
Device Name: | THE O'NEIL STERILE FIELD URINARY CATHETER KIT |
Classification | Tray, Catheterization, Sterile Urethral, With Or Without Catheter (kit) |
Applicant | GO MEDICAL INDUSTRIES PTY. LTD. 200 CHURCHILL AVE. Subiaco, Perth, AU 6008 |
Contact | George O'neil |
Correspondent | George O'neil GO MEDICAL INDUSTRIES PTY. LTD. 200 CHURCHILL AVE. Subiaco, Perth, AU 6008 |
Product Code | FCM |
CFR Regulation Number | 876.5130 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2000-09-08 |
Decision Date | 2000-12-27 |