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DATEX ENGSTOM MANUAL RESUSCITATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K970991
510(k) Type
Traditional
Applicant
PROMEDIC, INC.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
6/16/1997
Days to Decision
89 days
Submission Type
Summary

DATEX ENGSTOM MANUAL RESUSCITATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K970991
510(k) Type
Traditional
Applicant
PROMEDIC, INC.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
6/16/1997
Days to Decision
89 days
Submission Type
Summary