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

XN CHECK

K Number: K160590 · Decision Dec 22, 2016
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
191
Applicant Total
33
Review Days
296

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Basic Information

Device Name
XN CHECK
K Number
K160590
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.8625
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Streck
Date Received
March 1, 2016
Decision Date
December 22, 2016
Product Code
JPK
Advisory Committee
Hematology
Review Advisory Committee
HE
Third Party
N

Classifications

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

Product Code Device Name
JPK Mixture, Hematology Quality Control

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Other Clearances by Streck

K Number Device Name
K254166 MDx-Chex for BCN
K231223 MDx-Chex for BC-GN
K231221 MDx-Chex for BC-GP
K170091 UA-Cellular Complete
K160588 XN CHECK BF
K160586 XN-L CHECK
K160585 XN CAL
K141957 XN CHECK BF
K141964 XN CHECK
K141962 XN CAL
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