FDA 510(k) FDA class 2 Substantially Equivalent 🇫🇮 Finland

Planmed Clarity

K Number: K163328 · Decision Dec 28, 2017
Classifications
1
FEI Numbers
40
Registration Numbers
40
Same Product Code
54
Applicant Total
20
Review Days
395

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Basic Information

Device Name
Planmed Clarity
K Number
K163328
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1715
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Planmed OY
Date Received
November 28, 2016
Decision Date
December 28, 2017
Product Code
MUE
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
MUE Full Field Digital, System, X-Ray, Mammographic

Similar 510(k) Clearances

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

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Other Clearances by Planmed OY

K Number Device Name
K250318 Planmed XFI
K211720 Planmed Clarity 2D, Planmed Clarify S
K213278 Planmed Verity
K192317 Planmed Clarity 2D and Clarity S
K180918 Planmed Verity
K143435 Planmed Verity
K121418 PLANMED VERITY
K121963 PLANMED NUANCE DIGIGUIDE
K042671 PLANMED SOPHIE NUANCE CLASSIC
K021945 PLANMED SOPHIE & SOPHIE CLASSIC (WITH DIGISPOT AND CYTOGUIDE)
Search all 20 clearances from Planmed OY →