FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Medline Microtek C-Flo Bag Decanter, Sterile (2000S); Medline Microtek Bag Decanter II, Sterile (2002S); Medline Microtek Vial Decanter, Sterile (2006S); Medline Microtek Transfer Device, Sterile (2008S)

K Number: K251676 · Decision Sep 16, 2025
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
205
Applicant Total
1
Review Days
109

Basic Information

Device Name
Medline Microtek C-Flo Bag Decanter, Sterile (2000S); Medline Microtek Bag Decanter II, Sterile (2002S); Medline Microtek Vial Decanter, Sterile (2006S); Medline Microtek Transfer Device, Sterile (2008S)
K Number
K251676
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Microtek Medical, LLC
Date Received
May 30, 2025
Decision Date
September 16, 2025
Product Code
LHI
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
Y

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LHI Set, I.V. Fluid Transfer

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