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MYOTEST DBS NERVE STIMULATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K890746
510(k) Type
Traditional
Applicant
BIOMETER INTL. A/S
Country
Denmark
FDA Decision
Substantially Equivalent
Decision Date
7/14/1989
Days to Decision
151 days

MYOTEST DBS NERVE STIMULATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K890746
510(k) Type
Traditional
Applicant
BIOMETER INTL. A/S
Country
Denmark
FDA Decision
Substantially Equivalent
Decision Date
7/14/1989
Days to Decision
151 days