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NEUROLINE, SUBDERMAL NEEDLE ELECTRODES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K020907
510(k) Type
Traditional
Applicant
MEDICOTEST A/S
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/14/2002
Days to Decision
86 days
Submission Type
Statement

NEUROLINE, SUBDERMAL NEEDLE ELECTRODES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K020907
510(k) Type
Traditional
Applicant
MEDICOTEST A/S
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/14/2002
Days to Decision
86 days
Submission Type
Statement