The following data is part of a premarket notification filed by Navarre Biomedical Ltd. with the FDA for Navarre Biomedical Universal Drainage Catheter Set.
Device ID | K932391 |
510k Number | K932391 |
Device Name: | NAVARRE BIOMEDICAL UNIVERSAL DRAINAGE CATHETER SET |
Classification | Catheter, Irrigation |
Applicant | NAVARRE BIOMEDICAL LTD. 705 TOWER DR. Hamel, MN 55340 |
Contact | Gregg S Sutton |
Correspondent | Gregg S Sutton NAVARRE BIOMEDICAL LTD. 705 TOWER DR. Hamel, MN 55340 |
Product Code | GBX |
CFR Regulation Number | 878.4200 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-05-18 |
Decision Date | 1994-01-27 |