FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

NAVARRE LOCKING PIGTAIL UNIVERSAL DRAINAGE CATHETER

K Number: K951907 · Decision May 15, 1995
Classifications
1
FEI Numbers
243
Registration Numbers
243
Same Product Code
76
Applicant Total
9
Review Days
21

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
NAVARRE LOCKING PIGTAIL UNIVERSAL DRAINAGE CATHETER
K Number
K951907
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4200
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Navarre Biomedical , Ltd.
Date Received
April 24, 1995
Decision Date
May 15, 1995
Product Code
GBX
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GBX Catheter, Irrigation

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GBX), ordered by most recent decision date.

View all

Other Clearances by Navarre Biomedical , Ltd.

K Number Device Name
K955110 NAVARRE PERCUTANEOUS BILIARY DRAINAGE
K955505 OPTI-DRAIN MULTI-USE DRAINAGE CATHETER
K945909 NAVARRE N-FUSER(TM) PERIPHERAL INFUSION CATHETER
K951475 NAVARRE UNIVERSAL DRAINAGE CATHETER
K943663 NAVARRE 600 ML DRAINAGE BAG
K942315 NAVARRE PERCUTANEOUS ACCESS SET
K933600 NAVARRE BIOMEDICAL TIP-LOCKING DRAINAGE CATHETERS
K932391 NAVARRE BIOMEDICAL UNIVERSAL DRAINAGE CATHETER SET