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

ROYCO MODEL 921 CELL COUNTER

K Number: K791867 · Decision Nov 5, 1979
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
129
Applicant Total
4
Review Days
45

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Basic Information

Device Name
ROYCO MODEL 921 CELL COUNTER
K Number
K791867
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.5200
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Royco Instruments
Date Received
September 21, 1979
Decision Date
November 5, 1979
Product Code
GKL
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
GKL Counter, Cell, Automated (Particle Counter)

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Other Clearances by Royco Instruments

K Number Device Name
K800104 ROYCO MODEL 951 CELL MIXER
K791644 ROYCO MODEL 371 SUPER DILUTOR
K790442 ISOTONIC DILUENT