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

HEMASPINNER

K Number: K811534 · Decision Aug 18, 1981
Classifications
1
FEI Numbers
4
Registration Numbers
4
Same Product Code
5
Applicant Total
18
Review Days
78

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Basic Information

Device Name
HEMASPINNER
K Number
K811534
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
864.5850
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Geometric Data, Div. Smithkline Corp.
Date Received
June 1, 1981
Decision Date
August 18, 1981
Product Code
GKJ
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
GKJ Spinner, Slide, Automated

Similar 510(k) Clearances

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Other Clearances by Geometric Data, Div. Smithkline Corp.

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