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KINESTIM MUSCLE STIMULATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K871472
510(k) Type
Traditional
Applicant
PROMATEK INDUSTRIES, LTD.
Country
Canada
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
6/29/1987
Days to Decision
76 days

KINESTIM MUSCLE STIMULATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K871472
510(k) Type
Traditional
Applicant
PROMATEK INDUSTRIES, LTD.
Country
Canada
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
6/29/1987
Days to Decision
76 days