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

EZ-RANGE

K Number: K941965 · Decision Apr 25, 1995
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
191
Applicant Total
9
Review Days
368

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
EZ-RANGE
K Number
K941965
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.8625
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Hematronix, Inc.
Date Received
April 22, 1994
Decision Date
April 25, 1995
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

Similar 510(k) Clearances

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

View all

Other Clearances by Hematronix, Inc.

K Number Device Name
K012243 MCC URICHECK ASSAYED LIQUID URINE MULTICONSTITUENT CONTROL
K993496 RETIC-QUINOX
K972710 QUANTIFY(901)
K960471 TRI-COUNT 20
K960005 TRI-COURT 20-T
K935343 CENTRIFIQ BLOOD CONTROL
K904461 METER TRAX
K902389 TRI-COUNT 16