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

RE-CELL SLIDE RECAP

K Number: K772139 · Decision Jan 5, 1978
Classifications
1
FEI Numbers
10
Registration Numbers
10
Same Product Code
34
Applicant Total
18
Review Days
52

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Basic Information

Device Name
RE-CELL SLIDE RECAP
K Number
K772139
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.5260
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Geometric Data, Div. Smithkline Corp.
Date Received
November 14, 1977
Decision Date
January 5, 1978
Product Code
JOY
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
JOY Device, Automated Cell-Locating

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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
K761207 HEMATRAK RBC MORPHOLOGY
K770680 HEMATRAK
K770550 ATYPIA PROFILE MONITOR
Search all 18 clearances from Geometric Data, Div. Smithkline Corp. →