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MCSEER/MICRO CONTROLLER SLD ST EEG EVENT RECORDER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K910279
510(k) Type
Traditional
Applicant
NEW ENGLAND MEDICAL INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/4/1991
Days to Decision
224 days

MCSEER/MICRO CONTROLLER SLD ST EEG EVENT RECORDER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K910279
510(k) Type
Traditional
Applicant
NEW ENGLAND MEDICAL INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/4/1991
Days to Decision
224 days