510(k) K972091

AMS FOREIGN BODY EXTRATOR by American Medical Systems, Inc. — Product Code FFL

K972091 is an FDA 510(k) premarket notification submitted by American Medical Systems, Inc. for the device "AMS FOREIGN BODY EXTRATOR". The FDA issued a decision of Substantially Equivalent on August 29, 1997. The device falls under product code FFL (Dislodger, Stone, Basket, Ureteral, Metal), a Class II device regulated under 21 CFR 876.4680. American Medical Systems, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 29, 1997
Date Received
June 4, 1997
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