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MODIFIED ADULT CRICOTHYROIDOTOMY KIT

Page Type
Cleared 510(K)
510(k) Number
K885139
510(k) Type
Traditional
Applicant
PERTRACH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/25/1989
Days to Decision
161 days

MODIFIED ADULT CRICOTHYROIDOTOMY KIT

Page Type
Cleared 510(K)
510(k) Number
K885139
510(k) Type
Traditional
Applicant
PERTRACH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/25/1989
Days to Decision
161 days