510(k) K860201

PARENTERAL ADMINISTRATION SET by Migada, Ltd. — Product Code FPA

K860201 is an FDA 510(k) premarket notification submitted by Migada, Ltd. for the device "PARENTERAL ADMINISTRATION SET". The FDA issued a decision of Substantially Equivalent on February 4, 1986. The device falls under product code FPA (Set, Administration, Intravascular), a Class II device regulated under 21 CFR 880.5440. Migada, Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 4, 1986
Date Received
January 22, 1986
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Set, Administration, Intravascular
Device Class
Class II
Regulation Number
880.5440
Review Panel
HO
Submission Type