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

ALSEVER'S SOLUTION (MODIFIED)

K Number: K810783 · Decision May 13, 1981
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
366
Applicant Total
75
Review Days
51

Basic Information

Device Name
ALSEVER'S SOLUTION (MODIFIED)
K Number
K810783
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
864.2220
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
DUTCHLAND LABORATORIES, INC.
Date Received
March 23, 1981
Decision Date
May 13, 1981
Product Code
KIT
Advisory Committee
Hematology
Review Advisory Committee
CH
Third Party
N

Classifications

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

Product Code Device Name
KIT Media And Components, Synthetic Cell And Tissue Culture

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K821919 POWDERED RPMI-1634 MEDIUM
K821918 POWDERED RPMI-1603 MEDIUM
K821917 WAYMOUTH'S POWDER MEDIUM
K821913 ISCOVE'S MODIFIED DULBECCO POWDER MEDIUM
K821911 S-MEM-JOKLIK'S POWDER
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