510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K771655Substantially Equivalent

Curity Peakometer

Kendall Research Center, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K771655 is the FDA 510(k) clearance record for CURITY PEAKOMETER, a class II device, cleared for Kendall Research Center on under FDA product code FFG (Device, Urine Flow Rate Measuring, Non-Electrical, Disposable). FDA records list 14 510(k) clearances for Kendall Research Center, from to . As of , FDA records show no recalls naming K771655.

Clearance record

Decision date
Received
(46 days to decision)
Product code
FFG Device, Urine Flow Rate Measuring, Non-Electrical, Disposable
Regulation
21 CFR 876.1800
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Kendall Research Center 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code FFG

Trailing 12 months

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

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