Becton Dickinson Interlink(Tm) Lever/Y Lock
FDA 510(k) K940697 · Bd Becton Dickinson Vacutainer Systems Preanalytic
510(k) numberK940697
Submission
- Device name
- Becton Dickinson Interlink(Tm) Lever/Y Lock
- Applicant
- Bd Becton Dickinson Vacutainer Systems Preanalytic
Franklin Lake, NJ, US - Received
- February 16, 1994
- Decision date
- August 30, 1994
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- FPA – Set, Administration, Intravascular
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 880.5440
- Specialty
- General Hospital
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| K993186 | Synercid, 15 Ug, BBL Sensi-DiscJTN · Traditional | 11/03/1999SE |
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Questions and answers
When was Becton Dickinson Interlink(Tm) Lever/Y Lock cleared by the FDA?
Becton Dickinson Interlink(Tm) Lever/Y Lock (K940697) received a 510(k) decision of Substantially Equivalent on August 30, 1994, 195 days after the submission was received.
What is the product code of K940697?
The FDA product code is FPA – Set, Administration, Intravascular, a Class II (moderate risk) device regulated under 21 CFR 880.5440.