510(k) K932074

MEDISYSTEMS APHERESIS NEEDLE WITH GUARD by Medisystems Corp. — Product Code FIE

K932074 is an FDA 510(k) premarket notification submitted by Medisystems Corp. for the device "MEDISYSTEMS APHERESIS NEEDLE WITH GUARD". The FDA issued a decision of Substantially Equivalent on February 18, 1994. The device falls under product code FIE (Needle, Fistula), a Class II device regulated under 21 CFR 876.5540. Medisystems Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 18, 1994
Date Received
April 28, 1993
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