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MODIFIED SPANTRON FRAME FREEZE

Page Type
Cleared 510(K)
510(k) Number
K895546
510(k) Type
Traditional
Applicant
SPANTRON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/13/1989
Days to Decision
61 days

MODIFIED SPANTRON FRAME FREEZE

Page Type
Cleared 510(K)
510(k) Number
K895546
510(k) Type
Traditional
Applicant
SPANTRON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/13/1989
Days to Decision
61 days