510(k) K952392

MLI SET by Medical Technologies of Georgia — Product Code FPA

K952392 is an FDA 510(k) premarket notification submitted by Medical Technologies of Georgia for the device "MLI SET". The FDA issued a decision of Substantially Equivalent on August 7, 1995. The device falls under product code FPA (Set, Administration, Intravascular), a Class II device regulated under 21 CFR 880.5440. Medical Technologies of Georgia has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 7, 1995
Date Received
May 22, 1995
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