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POSEIDON CARDIAC MONITORING SYSTEM (PCMS)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K964408
510(k) Type
Traditional
Applicant
Instromedix, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/23/1997
Days to Decision
261 days
Submission Type
Summary

POSEIDON CARDIAC MONITORING SYSTEM (PCMS)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K964408
510(k) Type
Traditional
Applicant
Instromedix, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/23/1997
Days to Decision
261 days
Submission Type
Summary