510(k) K932391

NAVARRE BIOMEDICAL UNIVERSAL DRAINAGE CATHETER SET by Navarre Biomedical , Ltd. — Product Code GBX

K932391 is an FDA 510(k) premarket notification submitted by Navarre Biomedical , Ltd. for the device "NAVARRE BIOMEDICAL UNIVERSAL DRAINAGE CATHETER SET". The FDA issued a decision of Substantially Equivalent on January 27, 1994. The device falls under product code GBX (Catheter, Irrigation), a Class I device regulated under 21 CFR 878.4200. Navarre Biomedical , Ltd. has at least 8 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 27, 1994
Date Received
May 18, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Catheter, Irrigation
Device Class
Class I
Regulation Number
878.4200
Review Panel
SU
Submission Type