510(k) K170228

Belimed Steam Sterilizer MST-H TOP 5000 by Belimed AG — Product Code FLE

K170228 is an FDA 510(k) premarket notification submitted by Belimed AG for the device "Belimed Steam Sterilizer MST-H TOP 5000". The FDA issued a decision of Substantially Equivalent on May 12, 2017. The device falls under product code FLE (Sterilizer, Steam), a Class II device regulated under 21 CFR 880.6880. Belimed AG has at least 2 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 12, 2017
Date Received
January 25, 2017
Clearance Type
Abbreviated
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Sterilizer, Steam
Device Class
Class II
Regulation Number
880.6880
Review Panel
HO
Submission Type