510(k) K926433

4.5F IMAGECATH(R) CORONARY ANGIOSCOPE, COV45 by Baxter Edwards — Product Code LYK

K926433 is an FDA 510(k) premarket notification submitted by Baxter Edwards for the device "4.5F IMAGECATH(R) CORONARY ANGIOSCOPE, COV45". The FDA issued a decision of Substantially Equivalent on March 23, 1993. The device falls under product code LYK (Angioscope), a Class II device regulated under 21 CFR 876.1500. Baxter Edwards has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 23, 1993
Date Received
December 23, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Angioscope
Device Class
Class II
Regulation Number
876.1500
Review Panel
CV
Submission Type