510(k) K921091

CHOLANGIOLAPCATH(TM) by Bd Becton Dickinson Vacutainer Systems Preanalytic — Product Code GBZ

K921091 is an FDA 510(k) premarket notification submitted by Bd Becton Dickinson Vacutainer Systems Preanalytic for the device "CHOLANGIOLAPCATH(TM)". The FDA issued a decision of Substantially Equivalent on May 6, 1992. The device falls under product code GBZ (Catheter, Cholangiography), a Class I device regulated under 21 CFR 878.4200. Bd Becton Dickinson Vacutainer Systems Preanalytic has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 6, 1992
Date Received
March 6, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

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