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TMD SAFETY SYRINGE (FA12 SERIES 3ML/FA13 SERIES 5ML)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022278
510(k) Type
Traditional
Applicant
Taiject Medical Device Co., Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/12/2002
Days to Decision
59 days
Submission Type
Summary

TMD SAFETY SYRINGE (FA12 SERIES 3ML/FA13 SERIES 5ML)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022278
510(k) Type
Traditional
Applicant
Taiject Medical Device Co., Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/12/2002
Days to Decision
59 days
Submission Type
Summary