510(k) K926433
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