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NEOTONUS MODEL 1000 MUSCLE STIMULATOR SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K973096
510(k) Type
Traditional
Applicant
NEOTONUS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/12/1998
Days to Decision
297 days
Submission Type
Summary

NEOTONUS MODEL 1000 MUSCLE STIMULATOR SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K973096
510(k) Type
Traditional
Applicant
NEOTONUS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/12/1998
Days to Decision
297 days
Submission Type
Summary