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MODIFIED ADULT CRICOTHYROIDOTOMY KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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