510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K873594Substantially Equivalent

Tif Fecal Test

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

K873594 is the FDA 510(k) clearance record for TIF FECAL TEST, a class I device, cleared for Devetec, Inc. on under FDA product code LEA (Preservative, Cytological). FDA records list 4 510(k) clearances for Devetec, Inc., from to . As of , FDA records show no recalls naming K873594.

Clearance record

Decision date
Received
(25 days to decision)
Product code
LEA Preservative, Cytological
Regulation
21 CFR 864.4010
Device class
Class I
Review panel
Pathology
Applicant
Devetec, Inc. P.O. Box 10275, Bradenton FL
Third party review
No

Clearances, product code LEA

Trailing 12 months

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

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