510(k) K760152

FILTER (7220&7221 MOBIN-UDDIN VENA CAVA) by Edwards Laboratories — Product Code DTK

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