510(k) K970021

RUSCH SUPRAPUBIC TRAY by Rusch, Inc. — Product Code KOB

K970021 is an FDA 510(k) premarket notification submitted by Rusch, Inc. for the device "RUSCH SUPRAPUBIC TRAY". The FDA issued a decision of Substantially Equivalent on February 7, 1997. The device falls under product code KOB (Catheter, Suprapubic (And Accessories)), a Class II device regulated under 21 CFR 876.5090. Rusch, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 7, 1997
Date Received
January 3, 1997
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Catheter, Suprapubic (And Accessories)
Device Class
Class II
Regulation Number
876.5090
Review Panel
GU
Submission Type