Last synced on 14 November 2025 at 11:06 pm

DATEX ENGSTOM MANUAL RESUSCITATOR

Page Type
Cleared 510(K)
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)
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