510(k) K013395
K013395 is an FDA 510(k) premarket notification submitted by Ferrania S.P.A. for the device "LIFEJET VIDEO LINK". The FDA issued a decision of Substantially Equivalent on October 30, 2001. The device falls under product code LMA (Digitizer, Image, Radiological), a Class II device regulated under 21 CFR 892.2030. Ferrania S.P.A. has at least 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 30, 2001
- Date Received
- October 15, 2001
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- Yes
Device Classification
- Device Name
- Digitizer, Image, Radiological
- Device Class
- Class II
- Regulation Number
- 892.2030
- Review Panel
- RA
- Submission Type