510(k) K896992

METAL URETERAL BASKET STONE DISLODGER by Annex Medical, Inc. — Product Code FFL

K896992 is an FDA 510(k) premarket notification submitted by Annex Medical, Inc. for the device "METAL URETERAL BASKET STONE DISLODGER". The FDA issued a decision of Substantially Equivalent on February 8, 1990. The device falls under product code FFL (Dislodger, Stone, Basket, Ureteral, Metal), a Class II device regulated under 21 CFR 876.4680. Annex Medical, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 8, 1990
Date Received
December 11, 1989
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