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TSX PRM PULMONARY RESUSCITATION MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K973347
510(k) Type
Traditional
Applicant
SPIRACLE TECHNOLOGY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/23/1998
Days to Decision
321 days
Submission Type
Summary

TSX PRM PULMONARY RESUSCITATION MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K973347
510(k) Type
Traditional
Applicant
SPIRACLE TECHNOLOGY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/23/1998
Days to Decision
321 days
Submission Type
Summary