FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

R&D GLU-LINE HEMATOLOGY CONTROL

K Number: K034048 · Decision Mar 10, 2004
Classifications
1
FEI Numbers
269
Registration Numbers
269
Same Product Code
492
Applicant Total
79
Review Days
71

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Basic Information

Device Name
R&D GLU-LINE HEMATOLOGY CONTROL
K Number
K034048
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1660
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
R&D Systems, Inc.
Date Received
December 30, 2003
Decision Date
March 10, 2004
Product Code
JJX
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

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

Product Code Device Name
JJX Single (Specified) Analyte Controls (Assayed And Unassayed)

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K Number Device Name
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K100050 R & D SYSTEMS XERET HEMATOLOGY CONTROL
K091433 R&D SYSTEMS TETIC-I PLUS HEMOTOLOGY CONTROL
K073178 HCT EXTENDED HEMATOLOGY CONTROL, MODEL HCT004
K072846 CSF AUTOMATED CONTROL, MODELS CSF001, CSF003
K072268 HC WBC HEMATOLOGY CONTROL, MODEL: WBC00S
K072096 CBC-5D PLUS RETICS HEMATOLOGY CONTROL, MODELS: 5DR03, 5DR04
K070334 R&D SICKLE QC CONTROL
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