510(k) K850112

OMNIMED IV SOLUTION ADMINISTRATION SET by Omni Intl., Inc. — Product Code FPA

K850112 is an FDA 510(k) premarket notification submitted by Omni Intl., Inc. for the device "OMNIMED IV SOLUTION ADMINISTRATION SET". The FDA issued a decision of Substantially Equivalent on February 22, 1985. The device falls under product code FPA (Set, Administration, Intravascular), a Class II device regulated under 21 CFR 880.5440. Omni Intl., Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 22, 1985
Date Received
January 14, 1985
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