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

CLINITEK AUTO 2000 REAGENT CASSETTE (LEUKOCYTES)

K Number: K873304 · Decision Sep 11, 1987
Classifications
1
FEI Numbers
84
Registration Numbers
84
Same Product Code
6
Applicant Total
158
Review Days
24

Basic Information

Device Name
CLINITEK AUTO 2000 REAGENT CASSETTE (LEUKOCYTES)
K Number
K873304
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
864.7675
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
MILES LABORATORIES, INC.
Date Received
August 18, 1987
Decision Date
September 11, 1987
Product Code
LJX
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
LJX Test, Urine Leukocyte

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