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THE SPANTRON FRAME FREEZE

Page Type
Cleared 510(K)
510(k) Number
K890477
510(k) Type
Traditional
Applicant
SPANTRON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/31/1989
Days to Decision
59 days

THE SPANTRON FRAME FREEZE

Page Type
Cleared 510(K)
510(k) Number
K890477
510(k) Type
Traditional
Applicant
SPANTRON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/31/1989
Days to Decision
59 days