510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K915411Substantially Equivalent

Dade Immunoadsorbed Factor IX Deficient Plasma

Baxter Diagnostics, Inc., Miami FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K915411 is the FDA 510(k) clearance record for DADE IMMUNOADSORBED FACTOR IX DEFICIENT PLASMA, a class II device, cleared for Baxter Diagnostics, Inc. on under FDA product code GJT (Plasma, Coagulation Factor Deficient). FDA records list 72 510(k) clearances for Baxter Diagnostics, Inc., from to . As of , FDA records show no recalls naming K915411.

Clearance record

Decision date
Received
(161 days to decision)
Product code
GJT Plasma, Coagulation Factor Deficient
Regulation
21 CFR 864.7290
Device class
Class II
Review panel
Hematology
Applicant
Baxter Diagnostics, Inc. P.O.Box 520672, Miami FL
510(k) summary
Summary
Third party review
No

Clearances, product code GJT

Trailing 12 months

FDA records hold no clearances under product code GJT in the trailing twelve months.

FDA records show no clearances under product code GJT in the twelve months to November 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code GJT, trailing twelve months
MonthClearances
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260
November 20260