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PowerPAK Syringe

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K220114
510(k) Type
Traditional
Applicant
Vault Paragon Group, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/25/2023
Days to Decision
376 days
Submission Type
Summary

PowerPAK Syringe

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K220114
510(k) Type
Traditional
Applicant
Vault Paragon Group, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/25/2023
Days to Decision
376 days
Submission Type
Summary