Last synced on 25 January 2026 at 3:41 am

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

Page Type
Cleared 510(K)
PDF
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
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