510(k) K870555

VAN-TEC PEDIATRIC SUPRAPUBIC CATHETER SET by Van-Tec, Inc. — Product Code KOB

K870555 is an FDA 510(k) premarket notification submitted by Van-Tec, Inc. for the device "VAN-TEC PEDIATRIC SUPRAPUBIC CATHETER SET". The FDA issued a decision of Substantially Equivalent on March 10, 1987. The device falls under product code KOB (Catheter, Suprapubic (And Accessories)), a Class II device regulated under 21 CFR 876.5090. Van-Tec, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 10, 1987
Date Received
February 10, 1987
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