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

CHART-TYPE MICRO HEMATOCRIT TUBE READER

K Number: K870511 · Decision Mar 16, 1987
Classifications
1
FEI Numbers
13
Registration Numbers
13
Same Product Code
14
Applicant Total
7
Review Days
39

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Basic Information

Device Name
CHART-TYPE MICRO HEMATOCRIT TUBE READER
K Number
K870511
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.6400
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Norfolk Scientific, Inc.
Date Received
February 5, 1987
Decision Date
March 16, 1987
Product Code
JPI
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
JPI Device, Hematocrit Measuring

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K Number Device Name
K902028 STATSPIN ILLUMINATED MICRO-HEMATOCRIT TUBE READER
K890669 STATSPIN HDL-CHOLESTEROL PRECIPITATING MICRO TUBE
K883185 SAFECRIT PLASTIC MICROHEMATOCRIT TUBES
K881254 STATSPIN DISPOSABLE ROTOR, PRODUCT #RD01
K864974 GENERAL PURPOSE CENTRIFUGE
K860172 QWIKSPIN (TM)