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DIAGNOSTIC ELECTROMYOGRAPHY NEEDLE ELECTRODE, DISPOSABLE HYPODERMIC NEEDLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001869
510(k) Type
Traditional
Applicant
MEDICOTEST A/S
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/18/2000
Days to Decision
90 days
Submission Type
Statement

DIAGNOSTIC ELECTROMYOGRAPHY NEEDLE ELECTRODE, DISPOSABLE HYPODERMIC NEEDLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001869
510(k) Type
Traditional
Applicant
MEDICOTEST A/S
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/18/2000
Days to Decision
90 days
Submission Type
Statement