510(k) K926217

TERUMO ANGIOGRAPHIC CATHETER FOR LAPOROSCOPIC USE by Terumo Medical Corp. — Product Code GBZ

K926217 is an FDA 510(k) premarket notification submitted by Terumo Medical Corp. for the device "TERUMO ANGIOGRAPHIC CATHETER FOR LAPOROSCOPIC USE". The FDA issued a decision of Substantially Equivalent on July 13, 1993. The device falls under product code GBZ (Catheter, Cholangiography), a Class I device regulated under 21 CFR 878.4200. Terumo Medical Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 13, 1993
Date Received
December 10, 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