510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K904912Substantially Equivalent

Transducer Protector

Filtertek, Inc., Hebron IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K904912 is the FDA 510(k) clearance record for TRANSDUCER PROTECTOR, a class II device, cleared for Filtertek, Inc. on under FDA product code FIB (Protector, Transducer, Dialysis). FDA records list 10 510(k) clearances for Filtertek, Inc., from to . As of , FDA records show no recalls naming K904912.

Clearance record

Decision date
Received
(65 days to decision)
Product code
FIB Protector, Transducer, Dialysis
Regulation
21 CFR 876.5820
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Filtertek, Inc. P.O. Box 310 Price Rd., Hebron IL
Third party review
No

Clearances, product code FIB

Trailing 12 months

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

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