510(k) K851453

HOSPAL FISTULA NEEDLE by Hospal Medical Corp. — Product Code FIE

K851453 is an FDA 510(k) premarket notification submitted by Hospal Medical Corp. for the device "HOSPAL FISTULA NEEDLE". The FDA issued a decision of Substantially Equivalent on April 29, 1985. The device falls under product code FIE (Needle, Fistula), a Class II device regulated under 21 CFR 876.5540. Hospal Medical Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 29, 1985
Date Received
April 11, 1985
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