510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K894045Substantially Equivalent

Modified Polychrome IV Stain

Devetec, Inc., Bradenton FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K894045 is the FDA 510(k) clearance record for MODIFIED POLYCHROME IV STAIN, a class I device, cleared for Devetec, Inc. on under FDA product code KFD (Aniline Blue). FDA records list 4 510(k) clearances for Devetec, Inc., from to . As of , FDA records show no recalls naming K894045.

Clearance record

Decision date
Received
(48 days to decision)
Product code
KFD Aniline Blue
Regulation
21 CFR 864.1850
Device class
Class I
Review panel
Hematology
Applicant
Devetec, Inc. P.O. Box 10275, Bradenton FL
Third party review
No

Clearances, product code KFD

Trailing 12 months

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

FDA records show no clearances under product code KFD in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code KFD, 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