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LIFELOG(TM)

Page Type
Cleared 510(K)
510(k) Number
K902962
510(k) Type
Traditional
Applicant
MODULAR INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/4/1990
Days to Decision
61 days

LIFELOG(TM)

Page Type
Cleared 510(K)
510(k) Number
K902962
510(k) Type
Traditional
Applicant
MODULAR INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/4/1990
Days to Decision
61 days