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

HEMASTAIN FIXATIVE

K Number: K760485 · Decision Aug 30, 1976
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
8
Applicant Total
18
Review Days
10

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Basic Information

Device Name
HEMASTAIN FIXATIVE
K Number
K760485
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
864.1850
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Geometric Data, Div. Smithkline Corp.
Date Received
August 20, 1976
Decision Date
August 30, 1976
Product Code
KQC
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
KQC Stains, Hematology

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Other Clearances by Geometric Data, Div. Smithkline Corp.

K Number Device Name
K841852 AUTOLYZER 800
K811534 HEMASPINNER
K791041 HEMATRAK ABNORMAL RECOGNITION
K791108 CONTEXT FILTER
K790816 HEMATRAK MODEL 480
K790042 STAIN, HEMASTAIN RETIC
K780577 PLATELETS/CU MM
K772139 RE-CELL SLIDE RECAP
K761207 HEMATRAK RBC MORPHOLOGY
K770680 HEMATRAK
Search all 18 clearances from Geometric Data, Div. Smithkline Corp. →