Last synced on 20 May 2022 at 11:05 pm

1ST RESPONSE INFANT MANUAL RESUSCITATOR, BAG RESEVOIR, 1ST RESPONSE PEDIATRIC MANUAL RESUSCITATOR, BAG RESERVOIR, 1ST RE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K991861
510(k) Type
Traditional
Applicant
SIMS PORTEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/18/2000
Days to Decision
231 days
Submission Type
Summary

1ST RESPONSE INFANT MANUAL RESUSCITATOR, BAG RESEVOIR, 1ST RESPONSE PEDIATRIC MANUAL RESUSCITATOR, BAG RESERVOIR, 1ST RE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K991861
510(k) Type
Traditional
Applicant
SIMS PORTEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/18/2000
Days to Decision
231 days
Submission Type
Summary