510(k) K760152
K760152 is an FDA 510(k) premarket notification submitted by Edwards Laboratories for the device "FILTER (7220&7221 MOBIN-UDDIN VENA CAVA)". The FDA issued a decision of Substantially Equivalent on July 19, 1976. The device falls under product code DTK (Filter, Intravascular, Cardiovascular), a Class II device regulated under 21 CFR 870.3375. Edwards Laboratories has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 19, 1976
- Date Received
- July 1, 1976
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Filter, Intravascular, Cardiovascular
- Device Class
- Class II
- Regulation Number
- 870.3375
- Review Panel
- CV
- Submission Type