510(k) K093993
K093993 is an FDA 510(k) premarket notification submitted by Infraredx, Inc. for the device "LIPISCAN IVUS IMAGING SYSTEM MODEL NIRS-MC7-70". The FDA issued a decision of Substantially Equivalent on June 30, 2010. The device falls under product code OGZ (Catheter, Intravascular, Plaque Morphology Evaluation), a Class II device regulated under 21 CFR 870.1200. Infraredx, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 30, 2010
- Date Received
- December 24, 2009
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Catheter, Intravascular, Plaque Morphology Evaluation
- Device Class
- Class II
- Regulation Number
- 870.1200
- Review Panel
- CV
- Submission Type
Catheter used for delivery of a sensing modality to a coronary or peripheral artery region for determination of atherosclerotic plaque characteristics. For examination of morphologic features of coronary or peripheral artery lesions or plaques.