510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K905664Substantially Equivalent

Vial Access Cannula

Baxter Healthcare Corporation, Round Lake IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K905664 is the FDA 510(k) clearance record for VIAL ACCESS CANNULA, a class II device, cleared for Baxter Healthcare Corp on under FDA product code FMI (Needle, Hypodermic, Single Lumen). FDA records list 570 510(k) clearances for Baxter Healthcare Corp, from to . As of , FDA records show no recalls naming K905664.

Clearance record

Decision date
Received
(87 days to decision)
Product code
FMI Needle, Hypodermic, Single Lumen
Regulation
21 CFR 880.5570
Device class
Class II
Review panel
General Hospital
Applicant
Baxter Healthcare Corp Rte. 120 And Wilson Rd., Round Lake IL
Third party review
No

Clearances, product code FMI

Trailing 12 months
12 clearances under product code FMI in the twelve months to November 2026, March 2026 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code FMI, trailing twelve months
MonthClearances
December 20250
January 20261
February 20260
March 20263
April 20261
May 20260
June 20261
July 20262
August 20263
September 20261
October 20260
November 20260