510(k) K914348

ER-1000 CATHERIZATION C-ARM SYSTEMS by Shimadzu Medical Systems — Product Code IYB

K914348 is an FDA 510(k) premarket notification submitted by Shimadzu Medical Systems for the device "ER-1000 CATHERIZATION C-ARM SYSTEMS". The FDA issued a decision of Substantially Equivalent on November 1, 1991. The device falls under product code IYB (Tube Mount, X-Ray, Diagnostic), a Class I device regulated under 21 CFR 892.1770. Shimadzu Medical Systems has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 1, 1991
Date Received
September 27, 1991
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Tube Mount, X-Ray, Diagnostic
Device Class
Class I
Regulation Number
892.1770
Review Panel
RA
Submission Type