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

ATYPIA PROFILE MONITOR

K Number: K770550 · Decision Jun 17, 1977
Classifications
1
FEI Numbers
59
Registration Numbers
59
Same Product Code
376
Applicant Total
18
Review Days
88

Basic Information

Device Name
ATYPIA PROFILE MONITOR
K Number
K770550
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
March 21, 1977
Decision Date
June 17, 1977
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

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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
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