Last synced on 4 February 2023 at 10:33 pm

EMERGENCY PERCUTANEOUS CRICOTHYROIDOTOMY KIT,MODIF

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