BAXTER REINFORCED EXPANDED PTFE STEPPED VASCULAR GRAFT— 510(k) K944844
UnknownBaxter Healthcare Corp
FDA 510(k) clearance K944844 for BAXTER REINFORCED EXPANDED PTFE STEPPED VASCULAR GRAFT, Unknown on 1995-03-31. Applicant: Baxter Healthcare Corp. Device class: 2.
Clearance details
- Applicant
- Baxter Healthcare Corp
- Product code
- Code DYF
- Device class
- Class 2
- Regulation
- 21 CFR 870.3450
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Traditional
- Location
- Irvine, CA, US
Recent devices under product code DYF
view allMore clearances from Baxter Healthcare Corp
view all- K190910 — PrisMax System Version 2
- K163530 — PrisMax Control Unit
- K130531 — ULTRAFUSE
- K132734 — NEUTRAL LUER ACTIVATED DEVICE (ONE-LINK NEEDLE-FREE IV CONNECTOR) AND EXTENSION SETS
- K130245 — LARGE BORE STOPCOCK WITH ROTATING MALE LUER LOCK/LARGE BORE STOPCOCK WITH EXTENSION SET, GANG LARGE BORE STOPCOCK MANIFO
Data sourced from openFDA. This site is unofficial and independent of the FDA.