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EMERGENCY PERCUTANEOUS CRICOTHYROIDOTOMY KIT,MODIF

Page Type
Cleared 510(K)
510(k) Number
K914743
510(k) Type
Traditional
Applicant
PERTRACH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/10/1992
Days to Decision
273 days
Submission Type
Statement

EMERGENCY PERCUTANEOUS CRICOTHYROIDOTOMY KIT,MODIF

Page Type
Cleared 510(K)
510(k) Number
K914743
510(k) Type
Traditional
Applicant
PERTRACH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/10/1992
Days to Decision
273 days
Submission Type
Statement