Last synced on 20 December 2024 at 11:05 pm

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
K924610
510(k) Type
Traditional
Applicant
ENGINEERED MEDICAL SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/6/1993
Days to Decision
207 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
K924610
510(k) Type
Traditional
Applicant
ENGINEERED MEDICAL SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/6/1993
Days to Decision
207 days
Submission Type
Statement