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ELECTROENCEPHALOGRAPH RECORDING SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K920127
510(k) Type
Traditional
Applicant
MEDELEC INTL. CORP.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
6/10/1992
Days to Decision
152 days
Submission Type
Statement

ELECTROENCEPHALOGRAPH RECORDING SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K920127
510(k) Type
Traditional
Applicant
MEDELEC INTL. CORP.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
6/10/1992
Days to Decision
152 days
Submission Type
Statement