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JUNCTIONAL EMERGENCY TREATMENT TOOL MODEL 30-0088

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K123194
510(k) Type
Traditional
Applicant
North American Rescue Products, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/3/2013
Days to Decision
84 days
Submission Type
Summary

JUNCTIONAL EMERGENCY TREATMENT TOOL MODEL 30-0088

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K123194
510(k) Type
Traditional
Applicant
North American Rescue Products, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/3/2013
Days to Decision
84 days
Submission Type
Summary