B-D Interlink Syringe Cannula
by Bd Becton Dickinson Vacutainer Systems Preanalytic 510(k)
Active
510(k) K920422
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK920422 | Date29 Apr 1992 | StatusActive |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Recalls
No FDA recalls on record, checked 22 Oct 2026.
Specification
- 510(k) Number
- FDA Product Code
- FMF
- Device Class
- Class II
- Regulation
- 21 CFR Part 880.5860
- Advisory Committee
- General Hospital
- FDA Decision
- SESE Substantially Equivalent
Overview
AI-generated summary, 6 Oct 2026
The B-D Interlink Syringe Cannula is a blunt plastic cannula designed for needleless access to vials and preslit injection sites. It is specifically intended for use with Abbott LifeShield, McGaw SafeLine, and Baxter InterLink systems.
This device is not compatible with conventional injection sites that are not preslit. It is authorized under FDA 510(k) clearance K920422.
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Questions
AI-generated answers, 6 Oct 2026
What is the primary purpose of the B-D Interlink Syringe Cannula?
The B-D Interlink Syringe Cannula is a blunt plastic device engineered to provide needleless access to vials and preslit injection sites, reducing the need for traditional needles during these procedures.
Which injection systems are compatible with this cannula?
This cannula is specifically designed for compatibility with Abbott LifeShield, McGaw SafeLine, and Baxter InterLink systems. It is not compatible with conventional injection sites that are not preslit.
What is the regulatory status of this device?
The B-D Interlink Syringe Cannula is authorized for use under FDA 510(k) clearance K920422, which was granted on April 29, 1992.