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

RABBIT COMPLEMENT

K Number: K812522 · Decision Sep 23, 1981
Classifications
1
FEI Numbers
1
Registration Numbers
1
Same Product Code
5
Applicant Total
75
Review Days
21

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Basic Information

Device Name
RABBIT COMPLEMENT
K Number
K812522
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.4100
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Dutchland Laboratories, Inc.
Date Received
September 2, 1981
Decision Date
September 23, 1981
Product Code
KTQ
Advisory Committee
Immunology
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
KTQ Reagent, Complement

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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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