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

ImPACT

K Number: K170209 · Decision Feb 23, 2017
Classifications
1
FEI Numbers
3
Registration Numbers
3
Same Product Code
7
Applicant Total
6
Review Days
30

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Basic Information

Device Name
ImPACT
K Number
K170209
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
882.1471
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Impact Applications, Inc.
Date Received
January 24, 2017
Decision Date
February 23, 2017
Product Code
POM
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

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

Product Code Device Name
POM Computerized Cognitive Assessment Aid For Concussion

Similar 510(k) Clearances

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

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Other Clearances by Impact Applications, Inc.

K Number Device Name
K231688 ImPACT Version 4
K202485 ImPACT Version 4
K181223 ImPACT
K170551 ImPACT Quick Test
DEN150037 ImPACT Computerized Neurocognitive Concussion Management Aid