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TECA MYOJECT DISPOSABLE NEEDLE ELECTRODES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K973444
510(k) Type
Traditional
Applicant
MEDELEC, INC. D.B.A. TECA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/20/1997
Days to Decision
70 days
Submission Type
Summary

TECA MYOJECT DISPOSABLE NEEDLE ELECTRODES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K973444
510(k) Type
Traditional
Applicant
MEDELEC, INC. D.B.A. TECA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/20/1997
Days to Decision
70 days
Submission Type
Summary