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IMEX 8000 PERSONAL CASCULAR LAB

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K942243
510(k) Type
Traditional
Applicant
IMEX MEDICAL SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/3/1995
Days to Decision
543 days
Submission Type
Summary

IMEX 8000 PERSONAL CASCULAR LAB

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K942243
510(k) Type
Traditional
Applicant
IMEX MEDICAL SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/3/1995
Days to Decision
543 days
Submission Type
Summary