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

GEM Hemochron 100 System, GEM Hemochron 100 Activated Clotting Time Plus Test (ACT+), GEM Hemochron 100 Low Range Activated Clotting Time Test (ACT-LR), directCHECK ACT+ Whole Blood Control, Level 1 and Level 2, directCHECK ACT-LR Whole Blood Control, Level 1 and Level 2

K Number: K202101 · Decision Dec 29, 2021
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
180
Applicant Total
3
Review Days
518

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Basic Information

Device Name
GEM Hemochron 100 System, GEM Hemochron 100 Activated Clotting Time Plus Test (ACT+), GEM Hemochron 100 Low Range Activated Clotting Time Test (ACT-LR), directCHECK ACT+ Whole Blood Control, Level 1 and Level 2, directCHECK ACT-LR Whole Blood Control, Level 1 and Level 2
K Number
K202101
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.5425
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Accriva Diagnostics, Inc.
Date Received
July 29, 2020
Decision Date
December 29, 2021
Product Code
JPA
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
JPA System, Multipurpose For In Vitro Coagulation Studies

Similar 510(k) Clearances

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Other Clearances by Accriva Diagnostics, Inc.

K Number Device Name
K223352 Tenderfoot
K193041 Hemochron Signature Elite