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MODEL MK II TENS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K833251
510(k) Type
Traditional
Applicant
EUROPEAN ELECTRONIC SYSTEMS, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/5/1984
Days to Decision
164 days

MODEL MK II TENS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K833251
510(k) Type
Traditional
Applicant
EUROPEAN ELECTRONIC SYSTEMS, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/5/1984
Days to Decision
164 days