Navarre Biomedical , Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Navarre Biomedical , Ltd. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Navarre Biomedical , Ltd. has 9 FDA 510(k) cleared medical devices. Based in Hamel, US.
Historical record: 9 cleared submissions from 1994 to 1996. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Navarre Biomedical , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Navarre Biomedical , Ltd.
9 devices
Cleared
Nov 07, 1996
NAVARRE PERCUTANEOUS BILIARY DRAINAGE
Gastroenterology & Urology
365d
Cleared
Feb 07, 1996
OPTI-DRAIN MULTI-USE DRAINAGE CATHETER
General & Plastic Surgery
68d
Cleared
Jun 02, 1995
NAVARRE N-FUSER(TM) PERIPHERAL INFUSION CATHETER
Cardiovascular
182d
Cleared
May 15, 1995
NAVARRE LOCKING PIGTAIL UNIVERSAL DRAINAGE CATHETER
General & Plastic Surgery
21d
Cleared
Apr 24, 1995
NAVARRE UNIVERSAL DRAINAGE CATHETER
General & Plastic Surgery
25d
Cleared
Sep 08, 1994
NAVARRE 600 ML DRAINAGE BAG
Gastroenterology & Urology
42d
Cleared
Jul 08, 1994
NAVARRE PERCUTANEOUS ACCESS SET
General & Plastic Surgery
56d
Cleared
Mar 28, 1994
NAVARRE BIOMEDICAL TIP-LOCKING DRAINAGE CATHETERS
General & Plastic Surgery
244d
Cleared
Jan 27, 1994
NAVARRE BIOMEDICAL UNIVERSAL DRAINAGE CATHETER SET
General & Plastic Surgery
254d