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OMNITECH FULGURATING ELECTRODE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K050454
510(k) Type
Traditional
Applicant
Omnitech Systems, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/27/2005
Days to Decision
94 days
Submission Type
Statement

OMNITECH FULGURATING ELECTRODE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K050454
510(k) Type
Traditional
Applicant
Omnitech Systems, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/27/2005
Days to Decision
94 days
Submission Type
Statement