Last synced on 24 June 2022 at 11:05 pm

LIFELOG(TM)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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