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

HYCEL COUNTER 211

K Number: K782102 · Decision Jan 3, 1979
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
129
Applicant Total
22
Review Days
16

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Basic Information

Device Name
HYCEL COUNTER 211
K Number
K782102
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.5200
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Hycel, Inc.
Date Received
December 18, 1978
Decision Date
January 3, 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 Hycel, Inc.

K Number Device Name
K802422 HYCEL TRIGYCERIDE II TEST
K790335 HYCEL M
K782116 KETOSTEROID TEST, HYCEL-17
K782176 HYCEL LDH-INT TEST
K782100 HYCEL COUNTER 333
K782101 HYCEL COUNTER 222
K781004 HMA URIC ACID TEST
K780946 ROYCO MODEL 970 HEMATOLOGY DATA ANALYZER
K780464 LELECTIVE KINETIC SYSTEM-60
K780262 DIRECT UREA NITROGEN TEST
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