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

CELL-DYN RAPID-LYSE AND HEMOGLOBLIN

K Number: K881242 · Decision Apr 21, 1988
Classifications
1
FEI Numbers
1
Registration Numbers
1
Same Product Code
1
Applicant Total
28
Review Days
36

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Basic Information

Device Name
CELL-DYN RAPID-LYSE AND HEMOGLOBLIN
K Number
K881242
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.7500
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Abbott Diagnostics
Date Received
March 16, 1988
Decision Date
April 21, 1988
Product Code
GJZ
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
GJZ Cyanomethemoglobin Reagent And Standard Solution

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K Number Device Name
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K972182 ABBOTT STREP A CONTROLS
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K890491 CELL-DYN 3000 MULTI-PARAMETER HEMATOLOGY ANALYER
K881130 CELL-DYN ISOTONIC DILUENT
K873348 CELL-DYN DIFF SCREEN, AUTO. & SEMI AUTO. LYTIC AG.
K873347 CELL-DYN DIFF. SCREEN ISOTONIC DILUENT
K873408 MODEL 690 SPECTROPHOTOMETER
K872761 CELL-DYN 610 HEMATOLOGY ANALYZER
K870233 CELL-DYN 1600 MULTIPARAMETER AUTO. HEMA. ANALYZER
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