510(k) K924027

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

K924027 is an FDA 510(k) premarket notification submitted by Annex Medical, Inc. for the device "DISLODGER, STONE, BASKET, URETERAL, METAL". The FDA issued a decision of Substantially Equivalent on October 20, 1992. 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
October 20, 1992
Date Received
August 11, 1992
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