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AUTOPAK FERRITIN TEST DELIVERY SYS

Page Type
Cleared 510(K)
510(k) Number
K823275
510(k) Type
Traditional
Applicant
MICROMEDIC SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/3/1982
Days to Decision
30 days

AUTOPAK FERRITIN TEST DELIVERY SYS

Page Type
Cleared 510(K)
510(k) Number
K823275
510(k) Type
Traditional
Applicant
MICROMEDIC SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/3/1982
Days to Decision
30 days