510(k) K914111

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

K914111 is an FDA 510(k) premarket notification submitted by Annex Medical, Inc. for the device "METAL URETERAL BASKET STONE DISLODGER, HELICAL". The FDA issued a decision of Substantially Equivalent on February 28, 1992. The device falls under product code FGO (Dislodger, Stone, Flexible), 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 28, 1992
Date Received
September 13, 1991
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Dislodger, Stone, Flexible
Device Class
Class II
Regulation Number
876.4680
Review Panel
GU
Submission Type