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DUOPRO SAFETY SYRINGE (DUOPROSS)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022806
510(k) Type
Special
Applicant
M.K. MEDITECH CO. LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/19/2002
Days to Decision
27 days
Submission Type
Summary

DUOPRO SAFETY SYRINGE (DUOPROSS)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022806
510(k) Type
Special
Applicant
M.K. MEDITECH CO. LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/19/2002
Days to Decision
27 days
Submission Type
Summary