510(k) K922678

LOOP RETRIEVER by Annex Medical, Inc. — Product Code FFL

K922678 is an FDA 510(k) premarket notification submitted by Annex Medical, Inc. for the device "LOOP RETRIEVER". The FDA issued a decision of Substantially Equivalent on August 25, 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
August 25, 1992
Date Received
June 4, 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