Last synced on 20 May 2022 at 11:05 pm

IST RESPONSE MANUAL RESUSCITATOR, MODELS, 008000, 008003,008006

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K992057
510(k) Type
Traditional
Applicant
SIMS PORTEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/13/1999
Days to Decision
87 days
Submission Type
Summary

IST RESPONSE MANUAL RESUSCITATOR, MODELS, 008000, 008003,008006

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K992057
510(k) Type
Traditional
Applicant
SIMS PORTEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/13/1999
Days to Decision
87 days
Submission Type
Summary