510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K935307Substantially Equivalent

Dade(r) Thrombin-Antithrombin (Tat) Complex Elisa

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

K935307 is the FDA 510(k) clearance record for DADE(R) THROMBIN-ANTITHROMBIN (TAT) COMPLEX ELISA, a class II device, cleared for Baxter Diagnostics, Inc. on under FDA product code DDQ (Antigen, Antiserum, Control, Antithrombin Iii). FDA records list 72 510(k) clearances for Baxter Diagnostics, Inc., from to . As of , FDA records show no recalls naming K935307.

Clearance record

Decision date
Received
(385 days to decision)
Product code
DDQ Antigen, Antiserum, Control, Antithrombin Iii
Regulation
21 CFR 864.7060
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 DDQ

Trailing 12 months

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

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