510(k) K013037

EXCEL A.V FISUTAL NEEDLE SET by Exelint Intl. Co. — Product Code FIE

K013037 is an FDA 510(k) premarket notification submitted by Exelint Intl. Co. for the device "EXCEL A.V FISUTAL NEEDLE SET". The FDA issued a decision of Substantially Equivalent on December 7, 2001. The device falls under product code FIE (Needle, Fistula), a Class II device regulated under 21 CFR 876.5540. Exelint Intl. Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 7, 2001
Date Received
September 10, 2001
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Needle, Fistula
Device Class
Class II
Regulation Number
876.5540
Review Panel
GU
Submission Type