Last synced on 30 September 2022 at 11:05 pm

DIGITRACE(TM) HOME MONIT COMP/ELB(TM) EEG LUNCH BX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K910771
510(k) Type
Traditional
Applicant
NEW ENGLAND MEDICAL INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/18/1991
Days to Decision
299 days

DIGITRACE(TM) HOME MONIT COMP/ELB(TM) EEG LUNCH BX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K910771
510(k) Type
Traditional
Applicant
NEW ENGLAND MEDICAL INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/18/1991
Days to Decision
299 days