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1ST RESPONSE INTERMEDIATE MANUAL RESUSCITATOR

Page Type
Cleared 510(K)
510(k) Number
K023793
510(k) Type
Traditional
Applicant
PORTEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/11/2003
Days to Decision
90 days
Submission Type
Summary

1ST RESPONSE INTERMEDIATE MANUAL RESUSCITATOR

Page Type
Cleared 510(K)
510(k) Number
K023793
510(k) Type
Traditional
Applicant
PORTEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/11/2003
Days to Decision
90 days
Submission Type
Summary