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

RHESUS MONKEY BLOOD IN ALSEVER'S

K Number: K813512 · Decision Dec 29, 1981
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
3
Applicant Total
75
Review Days
14

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Basic Information

Device Name
RHESUS MONKEY BLOOD IN ALSEVER'S
K Number
K813512
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.3720
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Dutchland Laboratories, Inc.
Date Received
December 15, 1981
Decision Date
December 29, 1981
Product Code
LHW
Advisory Committee
Microbiology
Review Advisory Committee
PA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LHW Erythrocyte Suspension, Multi Species, Serological Reagent And Equipment

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K Number Device Name
K821913 ISCOVE'S MODIFIED DULBECCO POWDER MEDIUM
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K821918 POWDERED RPMI-1603 MEDIUM
K821917 WAYMOUTH'S POWDER MEDIUM
K821916 IMPROVED MEM-RICHTER'S POWDER MODIF.
K821919 POWDERED RPMI-1634 MEDIUM
K821911 S-MEM-JOKLIK'S POWDER
K821914 COON'S F-12 POWDER MEDIUM
K821915 BME AUTOCLAVABLE MEDIUM
K820926 E-BME POWDERED MEDIUM
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