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

QUICK-COUNT PLUS 2

K Number: K841504 · Decision Jun 11, 1984
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
129
Applicant Total
20
Review Days
62

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Basic Information

Device Name
QUICK-COUNT PLUS 2
K Number
K841504
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.5200
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Seragen Diagnostics, Inc.
Date Received
April 10, 1984
Decision Date
June 11, 1984
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)

Similar 510(k) Clearances

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Other Clearances by Seragen Diagnostics, Inc.

K Number Device Name
K872148 VIVID CHLAMYDIA(TM)
K851663 QUICK-COUNT HEMATOLOGY CONTROLS
K852260 QUICK-CHEM CALIBRATION SET
K851520 CK/LD ISOENZYMES CONTROLS(HUMAN)
K851521 LD-1(IMMUNO) SEPARATION SET
K850209 QUICK-LYTE
K844743 SERATEST ENA(RNP/SM) DETERMINATION
K842563 SERATEST DNA DETERMINATION
K840793 CK/MB IMMUNO-ISOENZYME CONTROL SERUM
K840863 SERATEST RF LATEX DETERMINATION
Search all 20 clearances from Seragen Diagnostics, Inc. →