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BAXTER ADULT/PEDI INFANT SINGLE/USE MAN RESUSCIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K924671
510(k) Type
Traditional
Applicant
ENGINEERED MEDICAL SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/21/1993
Days to Decision
217 days
Submission Type
Statement

BAXTER ADULT/PEDI INFANT SINGLE/USE MAN RESUSCIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K924671
510(k) Type
Traditional
Applicant
ENGINEERED MEDICAL SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/21/1993
Days to Decision
217 days
Submission Type
Statement