FDA 510(k) FDA class 2 Substantially Equivalent 🇳🇱 Netherlands

HemoTrol WB - Low, HemoTrol WB - Normal, HemoTrol WB - High

K Number: K182744 · Decision Feb 1, 2019
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
14
Applicant Total
7
Review Days
126

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
HemoTrol WB - Low, HemoTrol WB - Normal, HemoTrol WB - High
K Number
K182744
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.8625
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Eurotrol B.V.
Date Received
September 28, 2018
Decision Date
February 1, 2019
Product Code
GGM
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
GGM Control, Hemoglobin

Similar 510(k) Clearances

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

View all

Other Clearances by Eurotrol B.V.

K Number Device Name
K192842 HemoTrol Duo Low, HemoTrol Duo Normal, HemoTrol Duo High
K152553 CueSee Hypoxic
K131595 EUROTROL GAS-ISE HCT QC AND EUROTROL GAS-ISE HCT LVM
K121467 EUROTROL HEMATOCRIT CONTROL
K121468 EUROTROL GAS-ISE METABOLITES
K060215 ALBU TROL, LOW, MODEL 108.001.002; ALBU TROL, HIGH 108.002.002