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

HEMATRAK ABNORMAL RECOGNITION

K Number: K791041 · Decision Sep 4, 1979
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
379
Applicant Total
18
Review Days
91

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Basic Information

Device Name
HEMATRAK ABNORMAL RECOGNITION
K Number
K791041
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.5220
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Geometric Data, Div. Smithkline Corp.
Date Received
June 5, 1979
Decision Date
September 4, 1979
Product Code
GKZ
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
GKZ Counter, Differential Cell

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GKZ), ordered by most recent decision date.

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Other Clearances by Geometric Data, Div. Smithkline Corp.

K Number Device Name
K841852 AUTOLYZER 800
K811534 HEMASPINNER
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
K770550 ATYPIA PROFILE MONITOR
Search all 18 clearances from Geometric Data, Div. Smithkline Corp. →