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ULTI GUARD HOME INSULIN SYRINGE CONTAINER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K021983
510(k) Type
Traditional
Applicant
ULTI MED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/16/2002
Days to Decision
90 days
Submission Type
Summary

ULTI GUARD HOME INSULIN SYRINGE CONTAINER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K021983
510(k) Type
Traditional
Applicant
ULTI MED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/16/2002
Days to Decision
90 days
Submission Type
Summary