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MEDSIM 300 PATIENT SIMULATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K935817
510(k) Type
Traditional
Applicant
DYNATECH/NEVADA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/18/1994
Days to Decision
47 days
Submission Type
Summary

MEDSIM 300 PATIENT SIMULATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K935817
510(k) Type
Traditional
Applicant
DYNATECH/NEVADA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/18/1994
Days to Decision
47 days
Submission Type
Summary