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CRICOTHYROTOMY TUBE

Page Type
Cleared 510(K)
510(k) Number
K983000
510(k) Type
Traditional
Applicant
POLAMEDCO, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/27/1999
Days to Decision
426 days
Submission Type
Summary

CRICOTHYROTOMY TUBE

Page Type
Cleared 510(K)
510(k) Number
K983000
510(k) Type
Traditional
Applicant
POLAMEDCO, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/27/1999
Days to Decision
426 days
Submission Type
Summary