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1ST RESPONSE MANUAL RESUSCITATOR, MODEL 85XX

Page Type
Cleared 510(K)
510(k) Number
K014115
510(k) Type
Traditional
Applicant
PORTEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/27/2002
Days to Decision
75 days
Submission Type
Summary

1ST RESPONSE MANUAL RESUSCITATOR, MODEL 85XX

Page Type
Cleared 510(K)
510(k) Number
K014115
510(k) Type
Traditional
Applicant
PORTEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/27/2002
Days to Decision
75 days
Submission Type
Summary