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

Page Type
Cleared 510(K)
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)
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