510(k) K854652

ANGIOMED URETERAL STONE DISLODGERS by Angiomed U.S., Inc. — Product Code FFL

K854652 is an FDA 510(k) premarket notification submitted by Angiomed U.S., Inc. for the device "ANGIOMED URETERAL STONE DISLODGERS". The FDA issued a decision of Substantially Equivalent on February 10, 1986. The device falls under product code FFL (Dislodger, Stone, Basket, Ureteral, Metal), a Class II device regulated under 21 CFR 876.4680. Angiomed U.S., Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 10, 1986
Date Received
November 19, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Dislodger, Stone, Basket, Ureteral, Metal
Device Class
Class II
Regulation Number
876.4680
Review Panel
GU
Submission Type