Last synced on 25 April 2025 at 11:05 pm

K-PACK II (HYPODERMIC NEEDLE) 23G X 1, MODEL KN-2325RB, K-PACK II NEEDLE (HYPODERMIC NEEDLE) 25G X 1, MODEL KN-2525RB, K

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K984576
510(k) Type
Traditional
Applicant
TERUMO EUROPE N.V.
Country
Belgium
FDA Decision
Substantially Equivalent
Decision Date
6/14/1999
Days to Decision
173 days
Submission Type
Summary

K-PACK II (HYPODERMIC NEEDLE) 23G X 1, MODEL KN-2325RB, K-PACK II NEEDLE (HYPODERMIC NEEDLE) 25G X 1, MODEL KN-2525RB, K

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K984576
510(k) Type
Traditional
Applicant
TERUMO EUROPE N.V.
Country
Belgium
FDA Decision
Substantially Equivalent
Decision Date
6/14/1999
Days to Decision
173 days
Submission Type
Summary