FDA 510(k) FDA class 2 Substantially Equivalent 🇹🇷 Türkiye

Flowart

K Number: K221473 · Decision Sep 26, 2022
Classifications
1
FEI Numbers
424
Registration Numbers
424
Same Product Code
1173
Applicant Total
4
Review Days
129

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Basic Information

Device Name
Flowart
K Number
K221473
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Asset Medikal Tasarim As.
Date Received
May 20, 2022
Decision Date
September 26, 2022
Product Code
FPA
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
FPA Set, Administration, Intravascular

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FPA), ordered by most recent decision date.

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Other Clearances by Asset Medikal Tasarim As.

K Number Device Name
K221481 NeutrArt
K201872 NeutrArt
K190806 Flowart