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DISPOSABLE HYPODERMIC EMG NEEDLE ELECTRODE TECHNOMED EUROPE VERSION AND PRIVATE LABELED

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K062437
510(k) Type
Traditional
Applicant
TECHNOMED EUROPE
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
2/16/2007
Days to Decision
189 days
Submission Type
Summary

DISPOSABLE HYPODERMIC EMG NEEDLE ELECTRODE TECHNOMED EUROPE VERSION AND PRIVATE LABELED

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K062437
510(k) Type
Traditional
Applicant
TECHNOMED EUROPE
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
2/16/2007
Days to Decision
189 days
Submission Type
Summary