510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K770423Substantially Equivalent

Urine Tester, Model No. 707

Brother Scientific Products, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K770423 is the FDA 510(k) clearance record for URINE TESTER, MODEL NO. 707, a class II device, cleared for Brother Scientific Products, Inc. on under FDA product code EXR (Urinometer, Mechanical). FDA records list 2 510(k) clearances for Brother Scientific Products, Inc. As of , FDA records show no recalls naming K770423.

Clearance record

Decision date
Received
(88 days to decision)
Product code
EXR Urinometer, Mechanical
Regulation
21 CFR 876.1800
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Brother Scientific Products, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code EXR

Trailing 12 months

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

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