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INTERTRON 4500, INTERTRON 5000, MASTERSTIM I-2

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K921612
510(k) Type
Traditional
Applicant
MEDSTAR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/18/1992
Days to Decision
137 days
Submission Type
Statement

INTERTRON 4500, INTERTRON 5000, MASTERSTIM I-2

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K921612
510(k) Type
Traditional
Applicant
MEDSTAR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/18/1992
Days to Decision
137 days
Submission Type
Statement