510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K812107Substantially Equivalent

Renalab Transducer Protector, .22 Micron

Renalab, Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K812107 is the FDA 510(k) clearance record for RENALAB TRANSDUCER PROTECTOR, .22 MICRON, a class II device, cleared for Renalab on under FDA product code FIB (Protector, Transducer, Dialysis). FDA records list one 510(k) clearance for Renalab. As of , FDA records show no recalls naming K812107.

Clearance record

Decision date
Received
(24 days to decision)
Product code
FIB Protector, Transducer, Dialysis
Regulation
21 CFR 876.5820
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Renalab 4221 Richmond Rd., NW, Walker MI
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