510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K052678Substantially Equivalent

Aq-830 Slim Body, Body Fat Monitor

Limax Electronics Co., Ltd., Flagstaff AZ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K052678 is the FDA 510(k) clearance record for AQ-830 SLIM BODY, BODY FAT MONITOR, a class II device, cleared for Limax Electronics Co., Ltd. on under FDA product code MNW (Analyzer, Body Composition). FDA records list one 510(k) clearance for Limax Electronics Co., Ltd. As of , FDA records show no recalls naming K052678.

Clearance record

Decision date
Received
(90 days to decision)
Product code
MNW Analyzer, Body Composition
Regulation
21 CFR 870.2770
Device class
Class II
Review panel
Cardiovascular
Applicant
Limax Electronics Co., Ltd. 2904 N. Boldt Dr., Flagstaff AZ
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MNW

Trailing 12 months

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

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