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MONOJECTT BLUNTIP I.V. ACCESS CANNULA WITH VIAL ACCESS PIN DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980062
510(k) Type
Traditional
Applicant
DAVIS & GECK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/20/1998
Days to Decision
72 days
Submission Type
Summary

MONOJECTT BLUNTIP I.V. ACCESS CANNULA WITH VIAL ACCESS PIN DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980062
510(k) Type
Traditional
Applicant
DAVIS & GECK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/20/1998
Days to Decision
72 days
Submission Type
Summary